Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferase.

In this data article we describe synthetic and characterisation data for four members of the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine (termed "RU-SKI") class of inhibitors of Hedgehog acyltransferase, including associated NMR spectra for final compounds. RU-SKI compounds were selected for synthesis based on their published high potencies against the enzyme target. RU-SKI 41 (9a), RU-SKI 43 (9b), RU-SKI 101 (9c), and RU-SKI 201 (9d) were profiled for activity in the related article "Click chemistry armed enzyme linked immunosorbent assay to measure palmitoylation by Hedgehog acyltransferase" (Lanyon-Hogg et al., 2015) [1]. (1)H NMR spectral data indicate different amide conformational ratios between the RU-SKI inhibitors, as has been observed in other 5-acyl-6,7-dihydrothieno[3,2-c]pyridines. The synthetic and characterisation data supplied in the current article provide validated access to the class of RU-SKI inhibitors.

Specification table

Value of the data

Validated synthetic route to substituted 5-acyl-6,7-dihydrothieno[3,2-c]pyridines.

The synthesised compounds can be used as inhibitors of Hedgehog acyltransferase (Hhat), termed “RU-SKI” inhibitors.

Synthetic data provides route for development of other Hhat inhibitors based on this molecular core with improved activity profiles.

NMR spectral data demonstrate biologically active RU-SKI compounds possess variable amide conformational preferences, which can be modulated.

Data

This article describes the synthesis and characterisation of four 5-acyl-6,7-dihydrothieno[3,2-c]pyridine (“RU-SKI”) inhibitors of Hedgehog acyltransferase (Hhat) which were employed in dose–response analysis in the related article “Click-chemistry armed enzyme linked immunosorbent assay to measure palmitoylation by Hedgehog acyltransferase” [1]. The RU-SKI inhibitors were identified and developed by Resh and co-workers [2], [3], and the compounds with the highest published potencies against Hhat were selected for synthesis. RU-SKI 41 (9a), RU-SKI 43 (9b), RU-SKI 101 (9c) and RU-SKI 201 (9d) were synthesised according to our previously reported synthetic strategy to access the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine core scaffold [4]. Inhibitors were analysed in our Click Chemistry Armed Enzyme Linked Immunosorbent Assay, displaying low- and sub-micromolar IC50 values against Hhat [1].

As demonstrated in our previous study of the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine core [4], the amide in the RU-SKI compounds also adopts two conformations (Fig. 1). The conformational preference is affected by non-covalent interactions between the amide carbonyl and neighbouring substituents [4]. Altered conformational ratios are observed in the 1H NMR data of the RU-SKI compounds (Table 1, Fig. 2, Fig. 6, Fig. 10, Fig. 14). The synthetic, characterisation and conformational data of compounds 9a–9d is reported here, along with NMR spectra of final RU-SKI inhibitors.

Fig. 1

E- and Z-amide conformations adopted by the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine core of the RU-SKI compounds.

Table 1

Amide conformational ratio data from RU-SKI inhibitors estimated by 1H NMR spectroscopy measured at 400 MHz in CDCl3 (Fig. 2, Fig. 6, Fig. 10, Fig. 14).

Compound	Observed E:Z
RU-SKI 41 (9a)	1:1
RU-SKI 43 (9b)	4:6
RU-SKI 101 (9c)	2:8
RU-SKI 201 (9d)	7:3

Fig. 2

1H NMR (400 MHz, CDCl3) of RU-SKI 41 (9a).

Fig. 6

1H NMR (400 MHz, CDCl3) of RU-SKI 43 (9b).

Fig. 10

1H NMR (400 MHz, CDCl3) of RU-SKI 101 (9c).

Fig. 14

1H NMR (400 MHz, CDCl3) of RU-SKI 201 (9d).

Experimental design, materials and methods

Materials

Materials and equipment were as previously described [4].

Abbreviations

EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide), PyBOP ((benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate), TEA (triethylamine), DIPEA (N,N-diisopropylethylamine), DMF (dimethylformamide), DCM (dichloromethane), HOBt (hydroxybenzotriazole), TFA (trifluoroacetic acid), chex (cyclohexane).

General procedures

Synthesis of RU-SKI 41, 43, 101 and 201 followed our previously reported synthetic strategy (Scheme 1) [4].

General procedure A (ethyl phenoxy acetate preparation)

2-Bromoethylacetate (0.66 mL, 5.99 mmol, 1 eq) was added dropwise to a solution of K2CO3 (1660 mg, 12.0 mmol, 2 eq) and phenol (5.99 mmol, 1 eq) in acetone (25 mL) and stirred at room temperature overnight. The reaction mixture was concentrated in vacuo then dissolved in brine and extracted with ethyl acetate. The combined organic layers were dried over Na2SO4 and the solvent removed in vacuo. The phenyl ether was used without further purification.

General procedure B (thiophene ethylamide preparation using sodium methoxide)

Phenoxyethyl acetate (3.91 mmol, 1 eq) was dissolved in methanol (20 mL), and sodium methoxide solution (0.5 M, 2.12 mL, 19.5 mmol, 5 eq) added dropwise to the reaction mixture. 2-(3-Thienyl)ethylamine (0.47 mL, 508 mg, 3.91 mmol, 1 eq) was added dropwise and stirred overnight at room temperature. The solvent was removed in vacuo and the resulting crude material was dissolved in brine, extracted with ethyl acetate and the combined organic layers washed with water. The organic layer was dried over Na2SO4, concentrated in vacuo and the crude residue purified by flash column chromatography.

General procedures C, D, E, F, and N

General procedures C, D, E, F, and N were performed as previously described [4].

General procedure G

General procedure G was performed as previously described [5].

General procedure H

General procedure G was performed as previously described [6].

General procedure I (ester hydrolysis of ethyl aminoacetate/preparation of ethyl amino acetic acid)

Boc-protected ethyl aminoacetate (0.15 mmol, 1 eq) was dissolved in THF (5 mL), lithium hydroxide (1 M solution, 0.4 mL, 0.40 mmol, 3.8 eq) added and the reaction stirred overnight at room temperature. If necessary, more lithium hydroxide was added to the reaction mixture in order to drive the reaction to completion. The reaction was acidified with concentrated hydrochloric acid (pH 2) and extracted in ethyl acetate. The combined organic layers were dried over Na2SO4, concentrated in vacuo, and purified by column chromatography or used without further purification.

General procedure J (coupling of the side chain using PyBOP) (RU-SKI 41/43)

The amine obtained from general procedure F (0.11 mmol, 1 eq) was added to a solution of the acid obtained from general procedure I (0.12 mmol, 1.1 eq), DIPEA (52 μL, 0.30 mmol, 2.75 eq) and PyBOP (56 mg, 0.11 mmol, 1 eq) in DCM (5 mL) and the reaction stirred overnight at room temperature. The reaction was quenched by addition of water and extracted in ethyl acetate. The combined organic layers were washed with water and brine, dried over Na2SO4, concentrated in vacuo, and purified by flash column chromatography.

General procedure K (coupling of the side chain using EDC/HOBt) (RU-SKI 101/201)

The amine obtained from general procedure F (0.043 mmol, 1 eq) and the Boc-protected acetic acid obtained from general procedure I (0.043 mmol, 1 eq) were dissolved in DMF (~2 mL). HOBt (5.8 mg, 0.043 mmol, 1 eq), DIPEA (15 μL, 0.086 mmol, 2 eq) and EDC (12.4 mg, 0.065 mmol, 1.5 eq) were added to the reaction mixture and the reaction stirred overnight at room temperature. DCM was added and the solution washed with aqueous LiCl (5% w/w) and brine. The organic layer was dried over Na2SO4, concentrated in vacuo, and purified by flash column chromatography.

General procedure L (Boc deprotection by TFA)

The amide obtained from general procedure J or K (0.049 mmol, 1 eq) was dissolved in 1:1 mixture of DCM and TFA (5 mL). Afterwards, the solvent was removed in vacuo and the residual was neutralised by saturated sodium hydrogen carbonate, extracted with DCM three times and dried over MgSO4. The required amine was isolated using strong cation exchange resin and eluted with ammonia (2 M) in methanol to recover the free amine, and purified by flash column chromatography.

General procedure M (Boc deprotection by HCl in dioxane)

The amide obtained from general procedure J or K (0.18 mmol, 1 eq) was stirred in 4 M HCl-Dioxane (~5 mL) for 2 h at room temperature. The solvent was removed in vacuo and the residue dissolved in ethyl acetate, washed with water and brine and dried over MgSO4. The required amine was isolated using strong cation exchange resin and eluted with ammonia (2 M) in methanol to recover the free amine, and purified by flash column chromatography.

General procedure N (coupling of the side chain using acid chlorides)

The amine obtained from general procedure F (0.09 mmol, 1 eq) and TEA (25 μL, 18 mg, 0.18 mmol, 2 eq) were dissolved in dry DCM (1 mL). The corresponding acid chloride (0.11 mmol, 1.2 eq) was added and the reaction mixture stirred at room temperature for 2 h. The solvent was removed in vacuo, and the residue purified by flash column chromatography.

RU-SKI synthetic data

RU-SKI 41 synthetic data

Ethyl (p-chlorophenoxy)acetate (1a)

The ethyl (p-chlorophenoxy)acetate (1a) was obtained from 4-chlorophenol (0.59 mL, 770 mg, 5.99 mmol, 1 eq) and 2-bromoethylacetate (1 g, 5.99 mmol, 1 eq) using general procedure A as a white solid (1.28 g, 5.87 mmol, 98%). 1H NMR (400 MHz, CDCl3) δ=7.31–7.22 (m, 2H), 6.91–6.82 (m, 2H), 4.61 (s, 2H), 4.29 (q, J=7.1 Hz, 2H), 1.31 (t, J=7.1 Hz, 3H); 13C NMR (101 MHz, CDCl3) δ=168.61, 156.46, 129.46, 126.70, 116.02, 65.63, 61.48, 14.15; IR υMAX (neat)/cm−1: 2986 (CH3, -CH2-, alkyl), 1755.14 (C=O stretch, ester), 1595.32, 1584.14, 1489.92, 1441.44, 1379.18, 1292.86, 1192.13, 1171.21, 1075.91, 1026.29, 1006.67, 929.80, 872.46, 719.30; HRMS (ESI, m/z) calcd. for C10H15NO3Cl+ [M+NH4]+, 232.0740; found, 232.0738 [M+NH4]+.

2-(p-Chlorophenoxy)-1-[2-(2-thienyl)ethylamino]-1-ethanone (2a)

The amide (2a) was obtained from 2-(3-thienyl)ethylamine (0.47 mL, 500 mg, 3.91 mmol, 1 eq) and ethyl (4-chlorophenoxy) acetate (850 mg, 3.91 mmol, 1 eq) using general procedure B as a white solid (975 mg, 3.30 mmol, 73%). 1H NMR (400 MHz, CDCl3) δ=7.31–7.26 (m, 2 H), 7.19 (dd, J=5.1, J=1.1 Hz, 1 H), 6.96 (dd, J=5.1, 3.4 Hz, 1 H), 6.87–6.79 (m, 3 H), 4.48 (s, 2 H), 3.65 (q, J=6.5 Hz, 2 H), 3.10 (t, J=6.7 Hz, 2 H); 13C NMR (101 MHz, CDCl3) δ=167.79, 155.72, 140.71, 129.69, 127.09, 125.51, 124.14, 115.93, 67.60, 40.28, 29.83. IR υMAX (neat)/cm−1: 3408.37, 3302.15, 3093.46, 3064.49, 2939.45, 2921.72, 2856.33 (CH3, -CH2-, alkyl), 1654.90 (C=O stretch, amide), 1597.10, 1537.80, 1488.72, 1427.34, 1342.82, 1278.53, 1230.48, 1171.54, 1096.68, 1046.50, 1007.56, 826.76, 698.54, HRMS (ESI, m/z) calcd. for C14H15NO2SCl+ [M+H]+, 296.0512; found, 296.0507 [M+H]+.

(p-Chlorophenoxy)(1-thia-5-aza-4,5,6,7-tetrahydroinden-4-yl)methane (4a) (ring closured imine 3a)/(amine 4a)

The cyclic imine (3a) was obtained from 2-(4-chlorophenoxy)-1-[2-(2-thienyl)ethylamino]-1-ethanone (2a) (348 mg, 1.18 mmol, 1 eq) using general procedure E as a brown oil (327 mg, 1.18 mmol, 100%). The crude material was used without further purification. 1H NMR (400 MHz, CDCl3) δ=δ 7.18–7.11 (m, 3 H), 7.04–6.99 (m, 3 H), 5.56 (s, 2 H), 4.11 (t, J=8.7 Hz, 2 H), 3.30 (t, J=8.7 Hz, 2 H). The amine (4a) was obtained from (4-chlorophenoxy)(1-thia-5-aza-6,7-dihydroinden-4-yl)methane (3a) (327 mg, 1.18 mmol, 1 eq) using general procedure F as yellow oil (181 mg, 0.65 mmol, 55%). 1H NMR (400 MHz, CDCl3) δ=7.28–7.23 (m, 2 H), 7.15 (d, J=5.2 Hz, 1 H), 6.91–6.87 (m, 3 H), 4.42–4.37 (m, 1 H), 4.22 (dd, J=9.1, J=3.8 Hz, 1 H), 4.05 (t, J=8.8 Hz, 1 H), 3.34 (dt, J=12.0, J=5.1 Hz, 1 H), 3.12 (ddd, J=12.0, J=7.2, 5.1 Hz, 1 H), 2.97–2.83 (m, 2 H).13C NMR (101 MHz, CDCl3) δ=157.36, 136.14, 133.22, 129.38, 125.91, 124.52, 122.58, 115.87, 70.87, 54.08, 41.31, 26.03. IR υMAX (neat)/cm−1: 3306.34 (-O-Ar, phenol), 3062.16, 2945.47, 2854.13 (-CH2-, alkyl), 1655.13 (N–H stretch, amine), 1596.82, 1583.67, 1537.80, 1488.44, 1368.75, 1313.41, 1286.47, 1171.28, 1139.99, 1099.45, 1087.64, 1057.58, 1007.72, 907.50, 854.11, 826.81, 805.72, 756.78, 699.55; HRMS (ESI, m/z), calcd. for C14H15NO2SCl+ [M+H]+, 296.0512; found, 296.0519 [M+H]+.

Ethyl (allylamino)acetate (5a)

The ethyl aminoacetate (5a) was obtained from ethyl bromoacetate (0.66 mL, 1000 mg, 5.99 mmol, 1 eq) and allylamine (8.7 mL, 116.2 mmol, 19.4 eq) using general procedure G as a colourless oil (137 mg, 0.96 mmol, 15%). The crude material was used without further purification. 1H NMR (400 MHz, CDCl3) δ=5.86 (ddt, J=16.3, J =10.2, 6.1 Hz, 1 H), 5.21–5.08 (m, 2 H), 4.18 (q, J=7.1 Hz, 2 H), 3.39 (s, 2 H), 3.26 (dt, J=6.1, J =1.4 Hz, 2 H), 1.86 (s, N–H), 1.26 (t, J=7.1 Hz, 3 H). 13C NMR (101 MHz, CDCl3) δ=172.51, 136.01, 116.99, 60.58, 51.64, 49.81, 14.67. IR υMAX (neat)/cm−1: 2983.57, 2939.32 (CH3, -CH2-, alkyl), 1747.22 (C=O stretch, ester), 1647.13, 1465.64, 1421.11, 1380.02, 1216.37, 1025.87, 941.38, 854.71; HRMS (ESI, m/z) calcd. for C7H14NO2+ [M+H]+, 144.1025; found 144.1018 [M+H]+.

Ethyl (N-allyl-N-tert-butoxycarbonylamino)acetate (6a)

The Boc protected ethyl aminoacetate (6a) was obtained from ethyl (allylamino)acetate (5a) (137 mg, 0.96 mmol, 1 eq) and di-tert-butyl dicarbonate (Boc2O) (209 mg, 0.96 mmol, 1 eq) using general procedure H as white solid (95 mg, 0.39 mmol, 40%). The crude material was used without further purification. 1H NMR (400 MHz, CDCl3) δ=5.76 (dd, J=10.8, J=5.9 Hz, 1 H), 5.17–5.07 (m, 2 H), 4.16 (qd, J=7.1, 2.3 Hz, 2 H), 3.95–3.91 (m, 2 H), 3.86 (d, J=5.7 Hz, 1 H), 3.80 (s, 1 H), 1.43 (s, 9 H) 1.25 (q, J=6.9 Hz, 3 H); 13C NMR (101 MHz, CDCl3) δ=(C=O too weak to be detected), 133.78, 133.69, 117.60, 116.80, 80.34, 60.96, 50.79, 50.34, 48.08, 47.74, 28.30, 28.25, 14.27, 14.16; IR υMAX (neat)/cm−1: 2978.90, 2933.91 (CH3, -CH2-, alkyl), 1751.62 (C=O stretch, ester), 1697.69 (C=O stretch, amide), 1434.77, 1396.05, 1366.58, 1246.43, 1192.20, 1165.13, 1143.63, 1028.45, 995.74, 971.72, 927.12, 887.08, 863.60, 775.82, 716.69; HRMS (ESI, m/z) calcd. for C14H24N2O4Na+ [M+CH3CN+Na]+, 307.1634; found, 307.1650 [M+CH3CN+Na]+.

(N-Allyl-N-tert-butoxycarbonylamino)acetic acid (7a)

The Boc protected aminoacetic acid (7a) was obtained from ethyl (N-allyl-N-tert-butoxycarbonylamino)acetate (6a) (37 mg, 0.15 mmol, 1 eq) using general procedure I as colourless oil (32 mg, 0.15 mmol, 97%). 1H NMR (400 MHz, CDCl3) δ 5.78 (dt, J=10.0, J=4.5 Hz, 1 H), 5.22–5.13 (m, 2 H), 4.01–3.93 (m, 2 H), 3.91 (d, J=5.8 Hz, 2 H), 1.47 (s, 9 H);13C NMR (101 MHz, CDCl3) δ=175.15, 174.59, 155.94, 155.14, 133.50, 133.27, 117.91, 117.20, 80.92, 80.80, 50.89, 50.23, 47.62, 28.26, 28.22; IR υMAX (neat)/cm−1: 3077.35, 2923.95, 2796.96 (CH3, -CH2-, Alkyl), 1678.95 (C=O stretch, carboxylic acid), 1643.04 (C=O stretch, amide), 1442.16, 1419.51, 1343.26, 1260.56, 1181.01, 1095.98, 993.81, 916.01; HRMS (ESI, m/z) calcd. for C10H17O4NNa+ [M+Na]+, 238.1050; found, 238.1043 [M+Na]+.

N-Allyl(2-{4-[(p-chlorophenoxy)methyl]-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl}-2-oxoethyl)amino 2,2-dimethylpropionate(8a)

The amide (8a) was obtained from (4-chlorophenoxy)(1-thia-5-aza-4,5,6,7-tetrahydroinden-4-yl)methane (4a) (82 mg, 0.29 mmol, 1 eq) and (N-allyl-N-tert-butoxycarbonylamino)acetic acid (7a) (69 mg, 0.32 mmol, 1.1 eq) using general procedure J as yellow oil (93 mg, 0.19 mmol, 67%). 1H NMR (400 MHz, CDCl3) δ=7.28–7.16 (m, 5 H), 7.15 (d, J=4.7 Hz, 1 H), 6.94 (d, J=5.2 Hz, 1 H), 6.85 (m, 5 H), 5.83 (s, 3 H), 5.31–4.94 (m, 5 H), 4.38 (s, 1 H), 4.25 (q, J=8.4, 6.6 Hz, 3 H), 4.18–3.83 (m, 10 H), 3.62 (m, 1 H), 3.08–2.77 (m, 5 H), 1.42 (s, 18 H); 13C NMR (101 MHz, CDCl3) δ=168.55, 167.90, 157.17, 156.73, 136.62, 134.08, 132.59, 130.43, 129.44, 129.33, 125.60, 124.82, 123.81, 123.30, 116.69, 116.04, 115.92, 115.74, 80.07, 69.56, 69.09, 60.39, 53.71, 50.86, 50.38, 50.27, 50.16, 47.87, 47.77, 40.92, 35.73, 28.33, 25.65, 24.76, 21.05, 14.20.

2-(Allylamino)-1-{4-[(p-chlorophenoxy)methyl]-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl}-1-ethanone (9a)

RU-SKI 41 (9a) was obtained from N-allyl(2-{4-[(p-chlorophenoxy)methyl]−1-thia−5-aza−4,5,6,7-tetrahydroinden−5-yl}−2-oxoethyl)amino 2,2-dimethylpropionate (8a) (86 mg, 0.18 mmol, 1 eq) using general procedure M as yellow oil (50 mg, 0.13 mmol, 73%). 1H NMR (400 MHz,CDCl3, rotameric ratio E:Z 1:1) δ 7.28–7.21 (m, 5 H), 7.18 (d, J=5.2 Hz, 1 H), 6.96 (d, J=5.2 Hz, 1 H), 6.92 (d, J=5.2 Hz, 1 H), 6.87–6.81 (m, 4 H), 5.99–5.86 (m, 3 H), 5.27–5.20 (m, 3 H), 5.14 (d, J=10.3 Hz, 2 H), 5.06–5.00 (m, 1 H), 4.25 (dt, J=7.2, 3.4 Hz, 2 H), 4.19–4.11 (m, 2 H), 4.05–3.98 (m, 1 H), 3.85 (d, J=16.1 Hz, 1 H), 3.72–3.52 (m, 6 H), 3.51 (s, 3 H), 3.32 (m, 4 H), 3.04 (qd, J=12.1, J=4.4 Hz, 2 H), 2.95 (m, 3 H), 2.89–2.81 (m, 2 H); 13C NMR (101 MHz, CDCl3) δ=171.08, 170.22, 157.14, 156.67, 136.64, 136.54, 136.39, 133.82, 132.57, 130.48, 129.52, 129.34, 126.45, 125.96, 125.56, 124.88, 123.90, 123.40, 116.52, 116.34, 115.91, 115.68, 69.59, 69.15, 53.64, 52.25, 52.20, 50.76, 50.05, 49.84, 40.61, 35.86, 25.64, 24.80; 13C NMR (DEPT) (101 MHz, CDCl3) δ=136.53, 136.39, 129.52, 129.34, 125.56, 124.88, 123.91, 123.41, 116.53, 116.35, 115.90, 115.67, 69.59, 69.14, 53.64, 52.25, 52.20, 50.76, 50.05, 49.83, 40.61, 35.86, 25.64, 24.80; IR υMAX (neat)/cm−1: 2905.66 (CH3, -CH2-, Alkyl), 1644.44 (C=O stretch, amide), 1491.88, 1427.41, 1284.32, 1242.08, 1212.27, 1170.89, 1092.26, 1046.83, 1006.02, 921.03, 825.66, 744.68, 710.72, 660.29; HRMS (ESI, m/z) calcd. for C19H21ClN2O2S+ [M+H]+, 377.1091; found, 377.1109 [M+H]+.

RU-SKI 43 synthetic data

Ethyl (m-tolyloxy)acetate (1b)

The ethyl (m-tolyloxy)acetate (1b) was obtained from m-cresol (0.63 mL, 0.65 mg, 5.99 mmol, 1 eq) and 2-bromoethylacetate (0.66 mL, 1000 mg, 5.99 mmol, 1 eq) using general procedure A as a white solid (1.09 g, 5.61 mmol, 93%). 1H NMR (400 MHz, CDCl3) δ=7.17 (t, J=7.9 Hz, 1 H), 6.81 (d, J=7.5 Hz, 1 H), 6.74 (s, 1 H), 6.70 (dd, J=8.2, J=2.4 Hz, 1 H), 4.60 (s, 2 H), 4.27 (q, J=7.1 Hz, 2 H), 2.32 (s, 3 H), 1.30 (t, J=7.2 Hz, 3 H), 13C NMR (101 MHz, CDCl3) δ=169.52, 158.28, 140.11, 129.71, 123.02, 116.05, 111.85, 65.85, 61.76, 21.94, 21.50; IR υMAX (neat)/cm−1: 2984.65, 2924.90 (CH3, -CH2-, Alkyl), 2924.90, 1758.38, 1734.58 (C=O, ester), 1586.99, 1489.76, 1442.80, 1378.32, 1275.60, 1261.07, 1200.37, 1156.26, 1088.71, 1029.60, 912.07, 857.19, 765.50, 750.32, 689.03; HRMS (ESI, m/z) calcd. for C11H15O3+ [M+H]+, 195.1021; found, 195.1023 [M+H]+.

1-[2-(2-Thienyl)ethylamino]-2-(m-tolyloxy)-1-ethanone (2b)

The amide (2b) was obtained from 2-(3-thienyl)ethylamine (0.48 mL, 522 mg, 4.08 mmol, 1 eq) and ethyl (m-tolyloxy)acetate (793 mg, 4.08 mmol, 1 eq) using general procedure B as a white solid (853 mg, 3.10 mmol, 76%). 1H NMR (400 MHz, CDCl3) δ=7.19 (d, J=7.8 Hz, 1 H), 7.16 (ddd, J=5.0, 3.0, J=1.0 Hz, 1 H), 6.94 (ddd, J=7.5, 5.1, J=3.4 Hz, 1 H), 6.86–6.82 (m, 1 H), 6.79–6.76 (m, 1 H), 6.71–6.65 (m, 2 H), 4.47 (s, 2 H), 3.62 (q, J=6.6 Hz, 2 H), 3.07 (t, J=6.7 Hz, 2 H), 2.34 (s, 3 H); 13C NMR (101 MHz, CDCl3) δ=168.36, 157.19, 142.21, 140.81, 129.51, 127.06, 125.49, 124.07, 122.93, 115.44, 111.53, 67.30, 43.63, 40.28, 29.91; IR υMAX (neat)/cm−1: 3103.09 (-O-Ar, br, phenol), 3046.00, 2922.20, 2860.65 (CH3, -CH2-, alkyl), 1663.53 (C=O stretch, amide), 1586.94, 1532.30, 1488.90, 1437.13, 1365.63, 1258.27, 1157.44, 1067.43, 920.48, 849.56, 824.35, 765.74, 750.20, 689.79; HRMS (ESI, m/z) calcd. for C15H18NO2S+ [M+H]+, 276.1058; found, 276.1071 [M+H]+.

(1-Thia-5-aza-4,5,6,7-tetrahydroinden-4-yl)(m-tolyloxy)methane (4b) (ring closured imine 3b)/(amine 4b)

The cyclic imine (1-thia-5-aza-6,7-dihydroinden-4-yl)(m-tolyloxy)methane (3b) was obtained from 1-[2-(2-thienyl)ethylamino]-2-(m-tolyloxy)-1-ethanone (2b) (807 mg, 2.93 mmol, 1 eq) using general procedure E as an orange oil (476 mg, 1.85 mmol, 63%). The crude material was used without further purification. 1H NMR (400 MHz, CDCl3) δ=7.33–7.25 (m, 1 H), 7.23–7.05 (m, 2 H), 7.03–6.93 (m, 1 H), 6.83 (s, 1 H), 6.83–6.75 (m, 1 H), 4.98 (s, 2 H), 3.91 (ddt, J=9.7, J=7.3, 1.2 Hz, 2 H), 2.92 (m, 2 H), 2.30 (s, 3 H). The cyclic amine (4b) was obtained from (1-thia-5-aza-6,7-dihydroinden-4-yl)(m-tolyloxy)methane (3b) (476 mg, 1.85 mmol, 1 eq) using general procedure F as a yellow solid (235 mg, 0.91 mmol, 49%). 1H NMR (400 MHz, CDCl3) δ=7.20 (t, J=7.9 Hz, 1 H), 7.14 (d, J=5.2 Hz, 1 H), 6.92 (d, J=5.2 Hz, 1 H), 6.81 (t, J=6.5 Hz, 3 H), 4.43–4.38 (m, 1 H), 4.24 (dd, J=9.2, J=3.8 Hz, 1 H), 4.11–4.06 (m, 1 H), 3.34 (dt, J=12.0, J=5.2 Hz, 1 H), 3.12 (ddd, J=12.1, J=6.9, 5.2 Hz, 1 H), 2.90 (tt, J=10.7, J=5.2 Hz, 2 H), 2.36 (s, 3 H), 2.31 (s, 1 H, N–H); 13C NMR (101 MHz, CDCl3) δ=158.74, 139.55, 136.00, 133.55, 129.23, 124.67, 122.42, 121.84, 115.44, 111.48, 70.30, 54.20, 41.23, 26.07, 21.54; IR υMAX (neat)/cm−1 2919.94, 2865.60, 2837.79 (alkyl, CH3, -CH2-), 1600.89 (N–H stretch, amine), 1584.04, 1488.99, 1466.59, 1433.15, 1382.23, 1359.82, 1326.95, 1311.57, 1290.14, 1259.12, 1170.61, 1156.70, 1132.10, 1047.23, 1032.89, 994.75, 879.52, 827.82, 769.24, 752.00, 711.74, 688.35; HRMS (ESI, m/z) calcd. for C15H18NOS+ [M+H]+, 260.1109; found, 260.1112 [M+H]+.

Ethyl (2-methylbutylamino)acetate (5b)

The ethyl aminoacetate (5b) was obtained from ethyl bromoacetate (166 μL 250 mg, 1.50 mmol, 1 eq) and 2-methyl butylamine (3.3 mL, 2.53 g, 29.04 mmol, 1 eq) using general procedure G. The crude material was purified by Isolera (SiO2; EtOAc:Hexane:TEA-12:88:1) and the expected compound was recovered as colourless oil (152 mg, 0.88 mmol, 58%).1H NMR (400 MHz, CDCl3) δ=4.16 (q, J=7.1 Hz, 2 H), 3.35 (s, 2 H), 2.59 (dd, J=12.6, J=5.5 Hz, 1 H), 2.52–2.46 (dd, J=11.2, J=7.1 Hz 1 H), 2.35 (dd, J=11.2, J=7.1 Hz, 1 H), 1.53–1.32 (m, 2 H), 1.25 (t, J=7.1 Hz, 3 H), 0.91–0.82 (m, 6 H); 13C NMR (101 MHz, CDCl3) δ=172.62, 60.65, 55.70, 51.24, 34.95, 27.32, 17.56, 11.23; HRMS (ESI, m/z) calcd. for C9H20NO2+ [M+H]+, 174.1494; found, 174.1497 [M+H]+.

Ethyl [N-tert-butoxycarbonyl(2-methylbutyl)amino]acetate (6b)

The Boc protected ethyl aminoacetate (6b) was obtained from ethyl (2-methylbutylamino)acetate (5b) (152 mg, 0.88 mmol, 1 eq) and di-tert-butyl dicarbonate (Boc2O) (427 mg, 1.955 mmol, 2.2 eq) using general procedure H. The crude material was purified by Isolera (SiO2; EtOAc:Hexane-2:8) and the expected compound was obtained as white solid (139 mg, 0.51 mmol, 57%). 1H NMR (400 MHz, CDCl3) δ 4.21 (qd, J=7.1, 3.1 Hz, 2 H), 4.02–3.90 (m, 1 H), 3.86 (s, 1 H), 3.20 (dd, J=14.2, J=6.7 Hz, 1 H), 3.08 (ddd, J=32.8, J=14.2, 8.0 Hz, 1 H), 1.62 (dd, J=13.7, J=5.7 Hz, 1 H), 1.47 (s, 9 H), 1.41 (d, J=6.3 Hz, 1 H), 1.30 (q, J=7.2 Hz, 3 H), 1.13 (dt, J=13.8, J=7.3 Hz, 1 H), 0.95–0.87 (m, 6 H); 13C NMR (101 MHz, CDCl3) δ=170.25, 170.11, 156.15, 155.57, 80.01, 79.92, 60.93, 54.39, 54.35, 49.99, 49.32, 34.26, 33.97, 28.35, 28.25, 27.41, 26.89, 17.03, 16.81, 14.26, 14.15, 11.31; IR υMAX (neat)/cm−1: 2966.24, 2932.72, 2877.14 (CH3, -CH2-, alkyl), 1753.57 (C=O stretch, ester), 1695.10 (C=O stretch, amide), 1456.93, 1403.46, 1365.89, 1245.03, 1192.65, 1174.47, 1145.09, 1096.17, 1029.26, 969.04, 930.01, 886.08, 863.78, 775.68; HRMS (ESI, m/z): calcd. for C16H30N2O4Na+ [M+CH3CN+Na]+, 337.2103; found, 337.2112 [M+CH3CN+Na]+.

[N-tert-Butoxycarbonyl(2-methylbutyl)amino]acetic acid (7b)

The Boc protected aminoacetic acid (7b) was obtained from ethyl [N-tert-butoxycarbonyl(2-methylbutyl)amino]acetate (6b) (51 mg, 0.19 mmol, 1 eq) using general procedure I as colourless oil (44 mg, 0.18 mmol, 95%). 1H NMR (400 MHz, CDCl3) δ=4.00 (d, J=4.0 Hz, 1 H), 3.92 (s, 1 H), 3.21 (dd, J=14.3, J=6.6 Hz, 1 H), 3.16–3.02 (m, 1 H), 1.64 (s, 1 H), 1.47 (s, 9 H), 1.42–1.25 (m, 1 H), 1.13 (dt, J=14.5, J=7.6 Hz, 1 H), 0.91 (m, 6 H); 13C NMR (101 MHz, CDCl3) δ=175.72, 174.65, 156.70, 155.49, 80.80, 80.38, 77.34, 77.23, 77.02, 76.88, 76.71, 54.62, 54.23, 49.50, 34.19, 33.94, 28.32, 28.23, 26.86, 16.96, 16.80, 11.29; IR υMAX (neat)/cm−1: 2965.36, 2933.32, 2877.19 (Alkyl, CH3, -CH2-), 1695.08 (br, C=O stretch merged together, carboxylic acid and carbamate), 1461.49, 1423.92, 1403.69, 1366.79, 1246.53, 1147.12, 1098.08, 969.73, 927.38, 871.21, 766.79; HRMS (ESI, m/z) calcd. for C14H26N2O4Na+ [M+CH3CN+Na]+, 309.1785; found, 309.1806 [M+CH3CN+Na]+.

(2-Oxo−2-{4-[(m-tolyloxy)methyl]−1-thia−5-aza−4,5,6,7-tetrahydroinden−5-yl}ethyl)(2-methylbutyl)amino 2,2-dimethylpropionate (8b)

The amide (8b) was obtained from (1-thia−5-aza−4,5,6,7-tetrahydroinden−4-yl)(m-tolyloxy)methane (4b) (31 mg, 0.12 mmol, 1 eq) and (7b) [N-tert-butoxycarbonyl(2-methylbutyl)amino]acetic acid (32.3 mg, 0.13 mmol, 1.1 eq) using general procedure J as yellow oil (21 mg, 0.045 mmol, 37%). 1H NMR (400 MHz, CDCl3) δ 7.23–7.13 (m, 4 H), 6.97 (d, J=5.3 Hz, 1 H), 6.91 (dd, J=15.3, 5.2 Hz, 1 H), 6.82 (t, J=6.2 Hz, 1 H), 6.77 (d, J=6.8 Hz, 2 H), 6.70 (d, J=8.0 Hz, 3 H), 5.31–5.22 (m, 1 H), 4.99 (dt, J=11.6, J=5.5 Hz, 1 H), 4.57–4.43 (m, 1 H), 4.37–4.23 (m, 3 H), 4.14 (m, 3 H), 3.69 (dd, J=17.9, J=7.2 Hz, 1 H), 3.35 (dtd, J=42.4, J=14.3, 7.6 Hz, 3 H), 3.23–2.76 (m, 6 H), 2.33 (s, 6 H), 1.54–1.25 (m, 25 H), 1.20–1.05 (m, 2 H), 0.92 (dp, J=9.8, 3.1 Hz, 12 H); 13C NMR (101 MHz, CDCl3) δ=171.14, 167.83, 158.59, 158.09, 156.42, 139.71, 139.45, 136.59, 133.76, 132.90, 130.68, 129.32, 129.15, 125.68, 124.90, 123.69, 123.10, 122.25, 121.77, 115.52, 115.38, 111.26, 111.04, 110.95, 79.99, 79.67, 69.31, 69.21, 68.93, 68.66, 54.29, 54.13, 53.73, 51.10, 49.27, 48.83, 40.97, 35.62, 34.05, 33.83, 28.40, 28.26, 27.00, 25.69, 24.80, 21.46, 17.12, 16.90, 11.45, 11.34; IR υMAX (neat)/cm−1: 2962.99, 2926.50, 2874.48 (CH3, -CH2-, alkyl), 1694.23 (C=O stretch, carbamate), 1661.69 (C=O stretch, amide), 1602.85, 1585.14, 1460.59, 1433.04, 1364.90, 1260.21, 1246.48, 1208.04, 1156.84, 1095.12, 1053.60, 968.15, 927.76, 878.13, 839.75, 765.50, 690.83; HRMS (ESI, m/z) calcd. for C27H39N2O4S+ [M+H]+, 487.2625; found, 487.2621 [M+H]+.

2-(2-Methylbutylamino)-1-{4-[(m-tolyloxy)methyl]-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl}-1-ethanone (9b)

RU-SKI 43 (9b) was obtained from N-allyl(2-{4-[(p-chlorophenoxy)methyl]-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl}-2-oxoethyl)amino 2,2-dimethylpropionate (8b) (15.8 mg, 0.033 mmol, 1 eq) using general procedure L as yellow oil (8.1 mg, 0.021 mmol, 62%). 1H NMR (400 MHz, CDCl3, rotameric ratio E:Z 4:6) δ=7.24–7.13 (m, 4 H), 6.98 (d, J=5.2 Hz, 1 H), 6.93 (d, J=5.2 Hz, 1 H), 6.82 (d, J=7.5 Hz, 1 H), 6.77 (d, J=7.6 Hz, 1 H), 6.73–6.67 (m, 4 H), 5.89 (t, J=4.7 Hz, 1 H), 5.27 (dd, J=8.8, J=4.1 Hz, 1 H), 5.01 (dd, J=12.8, J=4.5 Hz, 1 H), 4.31–4.24 (m, 2 H), 4.22–4.12 (m, 2 H), 4.06–4.00 (m, 1 H), 3.89 (dd, J=16.0, J=2.0 Hz, 1 H), 3.73–3.49 (m, 4 H), 3.07 (td, J=12.2, J=3.9 Hz, 1 H), 2.96 (dq, J=16.8, J=6.5, 5.7 Hz, 2 H), 2.87–2.81 (m, 1 H), 2.58 (tdd, J=9.7, 6.1, J=3.8 Hz, 2 H), 2.51–2.41 (m, 2 H), 2.34 (s, 3 H), 2.32 (s, 3 H), 1.54 (dddd, J=40.6, J=19.2, 12.0, 5.2 Hz, 4 H), 1.19 (dtd, J=14.8, J=7.4, 4.0 Hz, 2 H), 1.00–0.89 (m, 11 H); 13C NMR (101 MHz, CDCl3) δ=170.97, 170.18, 158.55, 158.05, 139.75, 139.47, 136.47, 133.69, 132.85, 130.76, 129.34, 129.15, 125.64, 124.97, 123.77, 123.19, 122.29, 121.81, 115.50, 115.28, 111.28, 111.04, 69.22, 68.66, 56.31, 53.73, 51.52, 50.96, 50.91, 40.68, 35.81, 35.02, 34.91, 27.43, 27.35, 25.65, 24.81, 21.46, 17.65, 17.57, 11.29, 11.21; HRMS (ESI, m/z) calcd. for C22H31N2O2S+ [M+H]+, 387.2101; found, 387.2109 [M+H]+.

RU-SKI 101 Synthetic Data

4-(m-Tolyl)-1-thia-5-aza-4,5,6,7-tetrahydroindene (4c)

The amine was synthesised as previously described [4].

2-(2-Methylbutylamino)-1-[4-(m-tolyl)-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl]-1-ethanone (8c)

The amide (8c) was obtained from 4-(m-tolyl)-1-thia-5-aza-4,5,6,7-tetrahydroindene (4c) (28 mg, 0.12 mmol, 1 eq) and [N-tert-butoxycarbonyl(2-methylbutyl)amino]acetic acid (7b) (30 mg, 0.12 mmol, 1 eq) using general procedure K as a yellow oil (35 mg, 0.08 mmol, 64%). Rf 0.14 (SiO2; EtOAc:Hex, 1:9). 1H NMR (400 MHz, CDCl3) δ 7.17 (m, 3 H), 7.11 (d, J=7.4 Hz, 1 H), 7.05 (d, J=7.6 Hz, 1 H), 6.84 (s, 1 H), 6.71 (s, 1 H), 4.33 (t, J=14.2 Hz, 1 H), 4.10–3.72 (m, 2 H), 3.39 (s, 1 H), 3.28–2.79 (m, 4 H), 2.33 (s, 3 H), 1.68 (s, 1 H), 1.49 (s, 6 H), 1.35 (s, 3 H), 1.28 (s, 1 H), 1.10 (s, 1 H), 0.96–0.74 (m, 6 H).13 C NMR, HRMS (ESI, m/z)

2-(2-Methylbutylamino)-1-[4-(m-tolyl)-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl]-1-ethanone (9c)

RU-SKI 101 (9c) was obtained from 2-(2-methylbutylamino)-1-[4-(m-tolyl)-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl]-1-ethanone (8c) (44 mg, 0.10 mmol, 1 eq) using general procedure L as yellow oil (18 mg, 0.05 mmol, 52%). 1H NMR (400 MHz, CDCl3, rotameric ratio E:Z 2 :8) δ= 7.27–6.98 (m, 7 H), 6.87 (s, 1 H), 6.77 (d, J=5.3 Hz, 1 H), 6.72 (d, J=5.2 Hz, 1 H), 5.90 (s, 1 H), 4.89 (d, J=8.9 Hz, 1 H), 3.81 (dd, J=14.1, J=5.0 Hz, 1 H), 3.53 (qd, J=15.8, J=4.4 Hz, 2 H), 3.37 (td, J=14.1, J=4.3 Hz, 1 H), 3.04 (ddd, J=16.8, J=11.4, 5.6 Hz, 2 H), 2.97–2.83 (m, 2 H), 2.58 (dt, J=11.2, J=5.6 Hz, 1 H), 2.45 (ddd, J=10.9, 7.2, J=2.5 Hz, 2 H), 2.33 (s, 4 H), 2.27–2.20 (m, N–H), 1.59 (dp, J=13.3, J=6.6 Hz, 1 H), 1.47 (dq, J=13.0, J=6.5, 5.6 Hz, 2 H), 1.19 (dt, J=14.6, J=6.5 Hz, 2 H), 0.93 (dt, J=14.8, J=7.0 Hz, 9 H); 13C NMR (101 MHz, CDCl3) δ=169.20, 144.73, 140.82, 138.15, 134.12, 134.00, 133.67, 129.35, 128.82, 128.62, 128.18, 126.63, 126.07, 125.77, 125.68, 124.50, 123.36, 123.28, 56.32, 54.02, 51.21, 38.51, 34.99, 34.96, 27.46, 27.36, 25.74, 21.48, 17.65, 11.34, 11.29; IR υMAX (neat)/cm−1: 2958.22, 2922.15, 2874.72 (CH3, -CH2-, alkyl), 1646.21 (C=O, amide), 1461.28, 1424.10, 1379.20, 1332.27, 1289.10, 1208.03, 1172.73, 1152.07, 1044.79, 892.05, 837.88, 810.68, 767.27, 736.91, 708.37; HRMS (ESI, m/z) calcd. for C21H29N2OS+ [M+H]+, 357.1995; found, 357.2019 [M+H]+.

RU-SKI 201 synthetic data

(6-Methyl-2-pyridyl)[2-(2-thienyl)ethylamino]formaldehyde (2d)

The amide (2d) was obtained from 2-(3-thienyl)ethylamine (390 uL, 424 mg, 3.31 mmol, 1 eq) and 6-methylpyridine-2-carboxylic acid (500 mg, 3.65 mmol, 1.1 eq) using general procedure C as a colourless oil (650 mg, 2.64 mmol, 72%). 1H NMR (400 MHz, CDCl3) δ=8.35 (s, 1 H, N–H), 8.02 (d, J=7.7 Hz, 1 H), 7.73 (t, J=7.7 Hz, 1 H), 7.28 (d, J=7.4 Hz, 1 H), 7.19 (d, J=5.1 Hz, 1 H), 7.00–6.96 (m, 1 H), 6.92 (d, J=3.2 Hz, 1 H), 3.77 (q, J=6.8 Hz, 2 H), 3.19 (t, J=7.0 Hz, 2 H), 2.56 (s, 3 H); 13C NMR (101 MHz, CDCl3) δ=164.55, 157.12, 149.11, 141.35, 137.46, 127.01, 125.87, 125.33, 123.85, 119.21, 40.86, 30.14, 24.25; IR υMAX (neat)/cm−1: 3256.7 (C–H stretch, Ar–H), 2920.3, 2902.4, 2824, 2806 (CH3, -CH2-, alkyl), 1667.66 (C=O stretch, amide), 1593.76, 1518.38, 1490.74, 1451.76, 1330.58, 1278.30, 1210.09, 1198.23, 1112.15, 1082.07, 1071.68.1052.13, 1025.33, 984.79, 931.22, 915.08, 901.76, 867.48, 853.24, 840.63, 823.83, 759.51, 726.94, 700.82, 686.66; HRMS (ESI, m/z) calcd. for C13H15N2OS+ [M+H]+, 247.0905; found, 247.0916 [M+H]+.

4-(6-Methyl-2-pyridyl)-1-thia-5-aza-4,5,6,7-tetrahydroindene (4d) (ring closured imine 3d)/(amine 4d)

The cyclic imine (3d) was obtained from (6-methyl-2-pyridyl)[2-(2-thienyl)ethylamino]formaldehyde (2d) (610 mg, 4.76 mmol, 1 eq) using general procedure E as a brown oil (478 mg, 2.10 mmol, 84%). The crude material was used without further purification. 1H NMR (400 MHz, CDCl3) δ=8.03 (d, J=7.6 Hz, 1 H), 7.82 (d, J=7.7 Hz, 1 H), 7.58 (d, J=5.2 Hz, 1 H), 7.02 (d, J=5.9 Hz, 1 H), 6.99 (dd, J=5.1, 3.4 Hz, 1 H), 4.08–4.03 (m, 2 H), 3.03–2.96 (m, 2 H), 2.29 (s, 3 H); The amine (4d) was obtained from 4-(6-methyl-2-pyridyl)-1-thia-5-aza-6,7-dihydroindene (3d) (468 mg, 2.05 mmol, 1 eq) using general procedure G as brown oil (281 mg, 1.22 mmol, 49% over two steps). 1H NMR (400 MHz, CDCl3) δ=7.52 (t, J=7.7 Hz, 1 H), 7.05 (dd, J=6.4, 3.2 Hz, 3 H), 6.98 (d, J=7.7 Hz, 1 H), 6.62 (d, J=5.2 Hz, 1 H), 5.15 (s, 1 H), 3.28 (dt, J=12.2, J=5.1 Hz, 1 H), 3.14 (ddd, J=12.3, J=7.6, 5.1 Hz, 1 H), 3.02–2.86 (m, 2 H), 2.57 (s, 3 H); 13C NMR (101 MHz, CDCl3) δ=161.30, 158.08, 136.70, 135.27, 135.18, 126.13, 122.00, 121.95, 119.29, 60.83, 41.90, 25.88, 24.51; IR υMAX (neat)/cm−1: 3289.25, 3044.04 (C–H stretch, Ar–H), 2923.00 (CH3, -CH2-, alkyl), 1592.05 (N–H stretch, amine), 1574.69 (N–H stretch, amine), 1442.07, 1372.97, 1260.56, 1208.46, 1158.68, 1146.21, 1123.21, 1090.07, 1032.98, 991.98, 934.93, 873.05, 851.80, 797.99, 766.03, 739.69, 712.11; HRMS (ESI, m/z) calcd. for C13H15N2S+ [M+H]+, 231.0950; found, 231.0959 [M+H]+.

{2-[4-(6-Methyl-2-pyridyl)-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl]-2-oxoethyl}(2-methylbutyl)amino 2,2-dimethylpropionate (8d)

The amide (8d) was obtained from 4-(6-methyl-2-pyridyl)-1-thia-5-aza-4,5,6,7-tetrahydroindene (4d) (5.5 mg, 0.024 mmol, 1 eq) and [N-tert-Butoxycarbonyl(2-methylbutyl)amino]acetic acid (7b) (5.8 mg, 0.024 mmol, 1 eq) using general procedure K as yellow oil (9.8 mg, 0.021 mmol, 90%),1H NMR (400 MHz, CDCl3) δ=7.52 (q, J=7.0, 6.4 Hz, 4 H), 7.16 (d, J=4.3 Hz, 3 H), 7.09 (t, J=6.6 Hz, 4 H), 6.89 (dd, J=24.5, 5.1 Hz, 4 H), 6.58 (s, 1 H), 6.01 (d, J=17.2 Hz, 2 H), 4.94 (dd, J=24.0, J=9.4 Hz, 1 H), 4.74–4.53 (m, 2 H), 4.09–4.02 (m, 1 H), 3.45 (dd, J=14.9, J=7.2 Hz, 1 H), 3.33–3.17 (m, 1 H), 3.15–3.09 (m, 1 H), 3.06–2.80 (m, 6 H), 2.58 (s, 5 H), 1.48 (s, 15 H), 1.11 (ddd, J=18.7, J =13.3, 6.1 Hz, 4 H), 0.90 (m, 10 H).

2-(2-Methylbutylamino)-1-[4-(6-methyl-2-pyridyl)-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl]-1-ethanone (9d)

RU-SKI 201 (9d) was obtained from {2-[4-(6-methyl-2-pyridyl)-1-thia-5-aza-4,5,6,7-tetrahydroinden-5-yl]-2-oxoethyl}(2-methylbutyl)amino 2,2-dimethylpropionate (8d) (7.7 mg, 0.017 mmol, 1 eq) using general procedure L as yellow oil (1.9 mg, 0.0053 mmol, 31%). 1H NMR (400 MHz, CDCl3, rotameric ratio E:Z 7:3) δ=7.53–7.47 (m, 2 H), 7.15 (t, J=6.9 Hz, 1 H), 7.07 (t, J=7.5 Hz, 1 H), 6.99 (d, J=7.4 Hz, 1 H), 6.88 (d, J=5.2 Hz, 1 H), 6.85 (d, J=5.1 Hz, 1 H), 6.79 (d, J=7.7 Hz, 1 H), 6.56 (s, 1 H), 5.96 (s, 1 H), 4.96–4.87 (m, 1 H), 4.21 (d, J=16.3 Hz, 1 H), 4.09–3.95 (m, 1 H), 3.83 (dd, J=16.3, J=4.0 Hz, 1 H), 3.60 (qd, J=16.3, J=15.9, 5.3 Hz, 1 H), 3.06–2.83 (m, 4 H), 2.70–2.39 (m, 8 H), 1.70–1.39 (m, 3 H), 1.17 (dddd, J=23.2, J=20.5, 15.5, 7.6 Hz, 2 H), 0.97–0.85 (m, 10 H); 13C NMR (101 MHz, CDCl3) δ=170.22, 169.70, 159.07, 158.88, 158.60, 137.06, 136.77, 135.78, 134.25, 133.06, 132.13, 126.73, 126.35, 123.72, 123.00, 122.67, 122.07, 119.00, 118.53, 58.90, 56.69, 56.43, 56.19, 51.41, 50.97, 40.85, 37.04, 35.07, 34.55, 31.09, 27.48, 27.39, 25.78, 25.00, 24.82, 24.64, 17.75, 17.60, 11.35, 11.29; IR υMAX (neat)/cm−1: 3401.51 (br, C–H stretch, Ar–H), 3004.68, 2920.3 (CH3, -CH2-, alkyl), 1660.01 (C=O stretch, amide), 1436.89, 1406.87, 1314.26, 1261.75, 1015.25, 951.75, 900.43, 702.76, 670.50; HRMS (ESI, m/z): calcd. for C20H28N3OS+ [M+H]+, 358.1963; found, 358.1953 [M+H]+.

NMR spectra

RU-SKI 41 NMR spectral data

See Fig. 2, Fig. 3, Fig. 4, Fig. 5.

Fig. 3

13C NMR (101 MHz, CDCl3) of RU-SKI 41 (9a).

Fig. 4

2D COSY (400 MHz, CDCl3) of RU-SKI 41 (9a).

Fig. 5

2D HSQC (400 MHz, CDCl3) of RU-SKI 41 (9a).

RU-SKI 43 NMR spectral data

See Fig. 6, Fig. 7, Fig. 8, Fig. 9.

Fig. 7

13C NMR (101 MHz, CDCl3) of RU-SKI 43 (9b).

Fig. 8

2D COSY (400 MHz, CDCl3) of RU-SKI 43 (9b).

Fig. 9

2D HSQC NMR (400 MHz, CDCl3) of RU-SKI 43 (9b).

RU-SKI 101 NMR spectral data

See Fig. 10, Fig. 11, Fig. 12, Fig. 13.

Fig. 11

13C NMR (101 MHz, CDCl3) of RU-SKI 101 (9c).

Fig. 12

2D COSY (400 MHz, CDCl3) of RU-SKI 101 (9c).

Fig. 13

2D HSQC (400 MHz, CDCl3) of RU-SKI 101 (9c).

RU-SKI 201 NMR spectral data

See Fig. 14, Fig. 15, Fig. 16, Fig. 17.

Fig. 15

13C NMR (101 MHz, CDCl3) of RU-SKI 201 (9d).

Fig. 16

2D COSY (400 MHz, CDCl3) of RU-SKI 201 (9d).

Fig. 17

2D HSQC (400 MHz, CDCl3) of RU-SKI 201 (9d).

Subject area	Chemistry
More specific subject area	Organic Synthesis
Type of data	Synthetic scheme, experimental procedures, physical data, NMR spectra
How data was acquired	NMR (Bruker AM-400 or AM-500). High resolution mass spectrometry (AUTOSPEC P673 spectrometer). Microwave reactions (Biotage Initiator)
Data format	Analysed
Experimental factors	N/A
Experimental features	Synthesis performed using standard organic chemistry techniques without inert atmosphere, unless otherwise stated.
Data source location	N/A
Data accessibility	Data are available in this article