Palladium-catalyzed intramolecular C-H arylation of 2-halo-N-Boc-N-arylbenzamides for the synthesis of N-H phenanthridinones.

A palladium catalyzed synthesis of N-H phenanthridinones was developed via C-H arylation. The protocol gives phenanthridinones regioselectively by one-pot reaction without deprotection. It exhibits broad substrate scope and affords targets in up to 95% yields. Importantly, it could be applied for the less reactive o-chlorobenzamides. This journal is © The Royal Society of Chemistry.

Introduction

Palladium-catalyzed direct functionalization of C–H bonds has become one of the most efficient and environmentally friendly mild procedures for building carbon–carbon bonds.[1] It holds a special place among various types of palladium-catalyzed coupling reactions. C–H direct arylation is its typical application, which is catalyzed by Pd(0) or Pd(ii) with phosphine ligands operating under a Pd(0)/Pd(ii) or Pd(ii)/Pd(iv) catalytic cycle with or without the assistance of base.[2] This coupling strategy has been well developed in terms of regioselectivity and efficiency; the tolerance of diverse functional groups makes the C–H arylation particularly versatile for organic synthesis. The starting materials may be easily achieved and thus this strategy has been used for building a variety of aromatic and heteroaromatic systems.[3]

Phenanthridinones are important structural units found in many natural products and pharmaceuticals that exhibit wide range of biological activities.[4] A variety of novel synthetic approaches have been developed to the synthesis of the phenanthridinone cores and related lactams, most of them are based on palladium catalyzed biaryl coupling by the regioselective C–H bond activation (Scheme 1a, synthesis of N-alkyl phenanthridinones).[5] Although they are effective for synthesis of N-alkyl phenanthridinones, the obvious drawbacks were observed when applied to N–H phenanthridinones.[5] Their scope of substrates is quite limited and high reaction temperature is necessary. To the best of our knowledge, only the yields with iodo-substituted anilides are reported. Usually a complex mixture of side-products is observed, decreasing the yield of desired product.[6] This is possibly resulted from the coordination of nitrogen to palladium in the presence of the NH free amide.[5] Earlier reported efficient protocols for such analog were mediated by potassium tert-butoxide[7] or photochemistry.[8,9] However, those procedures are not regioselective with substituted anilides due to radical cyclization mechanism (Scheme 1b, radical pathway for synthesis of N–H phenanthridinones), limiting application of substrate scopes.[7] So based on those disadvantages researchers reported utilization of protection groups which could be easily cleaved after the ring closure. Sandro Cacchi and co-workers[5] developed N-benzyl derivatives of N-benzoyl-o-iodoanilides which can be converted into the corresponding phenanthridinones in good to high yields, but needed one more deprotection step in TFA. François Tillequin et al.[6] developed Boc as protection and leaving group, however, one equivalent of Pd catalyst and two equivalents of phosphine ligands were involved, and only 26% yield was obtained.

Scheme 1

Synthesis of phenanthridinones via intramolecular cyclization.

In this account it is important to develop an operationally simple catalyst system for direct intramolecular arylation processes exhibiting broad scope for aryl chlorides, bromides, and iodides. Here we disclosed a palladium catalyzed one pot C–H activation protocol, cyclization and decarboxylation of N-Boc protected o-halobenzamides to produce phenanthridinones directly, which gave good to excellent yields as high as 95% (Scheme 1c, synthesis of N–H phenanthridinones by C–H activation from Boc protected amide). It can be easily scaled up even with increasing of yield. The reaction was promoted by Pd(t-Bu3P)2 combining together with KOAc, a convenient, commercial available catalyst inexpensive, but highly efficient to produce a broad range of phenanthridinones.

Results and discussion

The synthesis of the amide starting material 4xy for this investigation is shown in Scheme 2. Ortho-halogen substituted arylcarboxylic acid was easily converted to acyl chloride, which reacted with aniline to give amide 3xy. Then under catalytic amount of DMAP in DCM, 3xy was almost quantitatively converted to 4xy.[10]

Scheme 2

Synthesis of cyclization substrates.

In our initial investigation to optimize cyclization conditions of 4xy, we selected 4aa as starting point for screening, which is briefly summarized in Table 1. The C–H direct arylation is strongly dependent on the catalyst, the solvent and the base. Firstly we tried most popular coupling catalyst/base system (entries 1–3),[11] but obtained low yields; Pd(OAc)2/Bu3P/Ag2CO3 system[12] gave better yield (38%). After that, we tried Pd(PCy3)2 under various basic conditions, and found the yield can be increased to 48% when KOAc was used. Speculating that different ligand could be used to fine-tune the reaction due to its electronic and steric particularities,[2] we further screened Pd(t-Bu3P)2 catalyst[13] with different bases and finally identified Pd(t-Bu3P)2/KOAc was the best combination (entry 11, 72% yield). Other bases with different cation or anion were inferior (entries 9, 10). When the optimized condition was utilized with non-Boc protected substrate 3aa (entry 12), the strategy was not effective, suggesting that unprotected NH completely inhibited the reaction, presumably resulted by coordination of nitrogen to palladium in the presence of the NH free amide.[5]

Screening of reaction conditionsa

Entry	Catalyst/ligand (mol%)	Base (equiv.)	Subs. conv. (%)	Yieldb (%)
1	Pd(PPh3)4 (5)	K2CO3 (2)	100	22
2	Pd(OAc)2/PCy3·HBF4 (5/10)	Cs2CO3 (2)	100	33
3	Pd(OAc)2/Bu3P (5/10)	Ag2CO3 (2)	89	38
4	Pd(PCy3)2 (5)	Cs2CO3 (2)	97	35
5	Pd(PCy3)2 (5)	K2CO3	98	31
6	Pd(PCy3)2 (5)	AgOAc (4)	83	20
7	Pd(PCy3)2 (5)	K3PO4 (2)	88	11
8	Pd(PCy3)2 (5)	KOAc (4)	89	48
9	Pd(t-Bu3P)2 (5)	Cs2CO3 (2)	98	38
10	Pd(t-Bu3P)2 (5)	AgOAc (4)	82	23
11	Pd(t-Bu3P)2 (5)	KOAc (4)	100	72
12c	Pd(t-Bu3P)2 (5)	KOAc (4)	18	Trace

Reaction conditions: 4aa (0.5 mmol), Pd catalyst and base in DMA (5 ml) were heated at 120 °C for 90 min under Ar atmosphere.

Yield determined by LCMS.

3aa was used as substrate.

After optimization of the reaction condition, we attempted to extend the scope and generality of the intramolecular coupling as shown in Table 2. Various aryl acids and aryl amines were examined. Electron-rich groups (e.g. Me and OMe) either on the acid partner or on the aniline partner could smoothly undergo cyclization-decarboxylation which exclusively provided the desired products in 81–92% yields (entries 1–5). Notably, naphthyl-based substrates 4lb and 4lg also gave good to excellent yields (75–95%). 4lg gave lower yield due to slight electron deficiency. When this protocol was subjected to strong electron-deficient substrate such as cyano group (5jh, entry 8), the yield reduced sharply. To explore the cyclization position with respect to meta-substituted anilines, we tested meta-isopropyl aniline (entry 9). The reaction gave para and ortho-cyclization mixtures (2 : 1); However when tert-butyl analine was tested (entry 10), only para-cyclization was produced, presumably due to stronger steric hindrance. It was worth noting that the 3-amino thiophene also gave moderate to high yields (61–93%, entries 11–14), suggesting it's high C–H activation activity and regioselectivity. NMR confirmed the coupling is at second position. The reaction scope is not limited to benzoic acids, thiophene-carboxylic acids could also go cyclization smoothly (entries 15–20) with aniline or aminothiophene. Similar to early Pd-catalyzated protocol,[15] we found that pyridine ring was not an effective acid partner under our reaction condition (entries 21–23). To further evaluation the protocol's scaling up efficiency, we tested 4lb/4af/4kc as substrates for gram scale synthesis. To our delight, the yields increased up from 91%/84%/83% to 95%/93%/91% respectively.

Scope of phenanthridinones formationa

Entry	4xy	5xy	Yieldb [%]
1	4ab R1 = R2 = R3 = H R4 = OMe	5ab R1 = R2 = R3 = H R4 = OMe	88
2	4db R1 = Me R2 = R3 = H R4 = OMe	5db R1 = Me R2 = R3 = H R4 = OMe	81
3	4dc R1 = Me R2 = H R3 = Me R4 = OMe	5dc R1 = Me R2 = H R3 = Me R4 = OMe	87
4	4ec R1 = H R2 = OMe R3 = Me R4 = OMe	5ec R1 = H R2 = OMe R3 = Me R4 = OMe	92
5	4hd R1 = H R2 = F R3 = Cl R4 = OMe	5hd R1 = H R2 = F R3 = Cl R4 = OMe	89
6	4lb R1 = H R2 = OMe	5lb R1 = H R2 = OMe	91/95c
7	4lg R1 = Cl R2 = H	5lg R1 = Cl R2 = H	75
8			37d
9			78
10			82
11	4af R1 = R2 = H	5af R1 = R2 = H	84/93c
12	4df R1 = Me R2 = H	5df R1 = Me R2 = H	71
13	4ef R1 = H R2 = OMe	5ef R1 = H R2 = OMe	61
14			91
15	4kc R1 = Me R2 = OMe	5kc R1 = Me R2 = OMe	83/91c
16	4kg R1 =Cl R2 = H	5kg R1 =Cl R2 = H	71
17			84
18			85
19	4fb R1 = H R2 = OMe	5fb R1 = H R2 = OMe	62
20	4fc R1 = Me R2 = OMe	5fc R1 = Me R2 = OMe	58
21	4rc Y1 = C Y2 = N X = Br	5rc Y1 = C Y2 = N	0
22	4sc Y1 = N Y2 = C X = Br	5sc Y1 = N Y2 = C	0
23	4tc Y1 = N Y2 = C X = I	5tc Y1 = N Y2 = C	0

Reaction conditions: 1 mmol of substrate, 4 equiv. of KOAc, and 5% equiv. of Pd (t-Bu3P)2 in 10 ml DMA were heated at 120 °C for 2 h under Ar atmosphere.

Isolated yield.

Reaction conducted at 20 mmol scale.

Reacted at 135 °C.

Our above results showed that diverse functional groups, including F, Cl, CN, OMe, alkyl and a variety of aryl carboxylic acids and aryl amines were well tolerated. It leads us to speculate the reaction scope is not limited to bromo-substituted acid, but can also be extended to chloro-substituted acid. So we tested the activity of halogens in Table 3. Firstly, we selected the synthesis of 5aa as example (entries 1a to 1c). When iodide and bromide were tested, the reaction can be finished at 120 °C, given 77% and 66% yield respectively. When chloride was utilized, the yield decreased to moderate (45%) and must be conducted at higher temperature. After that, we tested electron-donating substitutes on either carboxylic moiety or aniline moiety (entries 2–5) and found yield can be as high as 78%; instead electron-withdrawing substitutes were negative to the reaction (entry 6, 38% yield). When the reaction was extended to strong electron withdrawing substituents, the yield decreased significantly even with iodide (entry 9). Chloro-thiophene carboxylic acid also delivered the corresponding products without a problem (entries 7, 8). Considering both chlorine and bromine were active as acid partner, we subjected 4uc for the reaction. Just as we predicted, the reaction turned to be quite messy and yielded no desired target (entry 10).

Scope of the reaction with respect to halogen-substituted substratesa

Entry	4xy	5xy	Yieldb [%]
1a	4aa1 X = I		77c
1b	4aa2 X = Br		66c
1c	4aa3 X = Cl		45
2			68
3			45
4			67
5			78
6			38
7			53
8			51
9			40
10			0

Reaction conditions: 1 mmol of substrate, 4 equiv. of KOAc, and 5% equiv. of (t-Bu3P)2Pd in 10 ml DMA were heated at 135 °C for 2 h under Ar atmosphere.

Isolated yield.

Reacted at 120 °C.

Next we examined the effect of catalyst loading to further optimize the reaction condition. Substrates 4lb and 4af were selected as examples which are shown in Table 4. Firstly we tested 4lb, when the catalyst loading increased from 5 mol% to 6 mol%, the influence was insignificant. However, when it was reduced to 4 mol%, the starting material remained and the yield was reduced by 13%; and only 60% yield was obtained when decreased further to 3 mol%; the same situation was observed with substrate 4af. Based on research below, 5 mol% catalyst was established as an optimal catalyst loading.

Effect of catalyst loadinga

Entry	Substrate	Pd(t-Bu3P)2	Subs. conv. (%)	Yield (%) of 5b
1	4lb	6%	100	93
2	4lb	5%	100	91
3	4lb	4%	94	78
4	4lb	3%	89	60
5	4af	5%	100	84
6	4af	4%	93	61
7	4af	3%	82	52

Reaction conditions: 1 mmol of substate, 4 equiv. of KOAc, Pd catalyst and 10 ml DMA were heated at 120 °C for 2 h under Ar atmosphere.

Isolated yield.

The directly cleavage of Boc was left for investigation for further exploring of reaction mechanism. We tested another protection group acetyl and used it for cyclization. However acetyl group is extremely unstable and only trace cyclization product was produced. It leaded us to suspect the stability of Boc on such conformationally rigid tricyclic system. So we re-protected the final target 5ec with Boc again and then heated it in the reaction system at same condition without Pd catalyst (Table 5). To our delight, 26% 5ec was produced and 69% 6ec remained. This result revealed that Boc was a fragile spot however just heating the substrate couldn't result full decomposition. Pd catalyst should have played a critical role in catalytic cycle for complete cleavage.

Stability testing of 6eca

Entry	Time (min)	5ec (%)b	6ec (%)b
1	60	13	83
2	90	26	69

Reaction conditions: 6ec (0.5 mmol), 4 equiv. of KOAc in DMA (5 ml) were heated at 120 °C.

Determined by LCMS.

Although additional data are needed to establish the mechanism, the fact that Pd catalyst loading influences the reaction significantly and the base KOAc gives the best yield, Boc group is some extend of fragile suggests their critical roles. It leads us to propose a plausible Pd(0)/Pd(ii) catalytic cycle[2] (Scheme 3). A proton abstraction mechanism previously proposed by Echavarren and Maseras,[16] was found to explain our reaction outcomes: (1) the anionic ligand KOAc is directly involved in C–H bond cleaving; (2) the anion ligand must bind to the catalyst, but not block the catalytic cycle by competitive occupation of vacant coordination sites;[17] (3) the arene which interacts with the catalyst weakly must compete for binding to the arylpalladium(ii) intermediate with the excess anionic ligand.[18] So initially oxidative addition of polarized Ph–Br bond to the Pd(0) catalyst forms a highly electrophilic arylpalladium intermediate I,[18,19] which exchange with KOAc to produce intermediate II,[18,20] followed by phosphine dissociation. Secondly Pd(ii) interacts with arene at the ortho position of aniline in a C–H activation manner which forms intermediate III.[20,21] Here HOAc plays a critical role in the stabilized coordination intermediate.[21,22] Next is irreversible deprotonation: Pd(ii) inserts into the C–H bond of the arene to give cyclobiarylpalladium intermediate IV,[20-22] accompanied by elimination of HOAc. Under the effect of produced HOAc, Pd presumably kicks off Boc and coordinates to nitrogen to give intermediate V, which finally undergoes reductive elimination to provide the desired product and regenerates the Pd(0) catalyst.[16,20,22]

Scheme 3

Proposed mechanism for the phenanthridinone synthesis.

Conclusions

In summary, we have developed a palladium catalyzed C–H arylation method for synthesis of N–H phenanthridinones from Boc protected diaryl amide. There are four advantages of using Boc as protection group: (1) the protection stage gives quantitive yield and just simple workup produces pure product; (2) the protection group is stable to some extent compared with acetyl group; (3) the coupling stage directly gives de-protection final targets, additional de-proctection is unnecessary; (3) in contrast to the system of radical pathway without protection reported by Bhakuni et al., the regioisomer is not a concern, only a single desired target was obtained. The catalyst Pd(t-Bu3P)2 is commercial available, inexpensive and the catalyst loading is reasonable; a second phosphine ligand is not required compared to published method.[6] This practical and convenient method can be easily scaled up, applicable for versatile substrates and produces high yields. Most important of all, it could be applied for the less reactive o-chlorobenzamides which greatly extend the substrates scope.

Experimental

General experimental details

Unless otherwise noted, all materials were obtained from commercial suppliers and used without further purification. The 1H and 13C NMR spectra were recorded on a Bruker Avance 400 spectrometer at 25 °C using DMSO-d6 or CDCl3 as the solvent. Chemical shifts (δ) are reported in ppm relative to Me4Si (internal standard), coupling constants (J) are reported in hertz, and peak multiplicity are reported as s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), or br s (broad singlet). High resolution mass analysis is performed on a Waters Q-TOF Premier mass spectrometer with electron spray ionization (ESI). Thin layer chromatography (TLC) was performed on 0.20 mm silica gel F-254 plates (Qingdao Haiyang Chemical, China). Visualization of TLC was accomplished with UV light and/or aqueous potassium permanganate or I2 in silica gel. Column chromatography was performed using silica gel 60 of 300–400 mesh (Qingdao Haiyang Chemical, China).

General procedure for synthesis of 4xy[10,23]

To suspension of 1x (5 mmol) in SOCl2 (5 ml) was added with 2 drops of DMF. The mixture was heated under reflux for 3 h. Then the mixture was concentrated and diluted with DCM and concentrated, then diluted and concentrated again to give light brown semi-solid. The residue was dissolved in anhydrous DCM (10 ml), added dropwise to a mixture of 2y (5 mmol) and Et3N (12.5 mmol) in DCM (10 ml). The resulting suspension was stirred for another 1 h after addition finished. The mixture was diluted with water, washed with 1 N HCl, 2 N NaOH and brine successively. The organic layer was dried over Na2SO4, filtered and concentrated to give the crude amide 3xy which was used for next step directly.

To the above crude 3xy was added anhydrous DCM (20 ml), DMAP (0.05 eq., 0.25 mmol), and Boc2O (1.2 eq., 6 mmol). The suspension was stirred until the bubbling was not observed which indication completion of the reaction. TLC showed a less polar product which was also confirmed by LCMS. The mixture was concentrated, diluted with hexane and water. After stirring for a couple of minutes a precipitate deposited. The solid was filtered, washed with water and hexane, dried under vacuum to give off-white solid 4xy.

General procedure for synthesis of product 5 (Tables 2 and 3)

To a 50 ml two necked flask equipped with a thermometer was added 4xy (1 mmol), DMA (10 ml), KOAc (4 eq., 4 mmol), Pd(t-Bu3P)2 (0.05 mmol, 0.05 eq.). The mixture was heated under argon at 120–135 °C for 2 h. It was diluted with H2O (30 ml), filtered and the solid was washed with H2O and ethanol successively. The crude product was dissolved in DCM/MeOH (5 : 1), filtered through celite to remove catalyst residue, then concentrated and re-crystallized from hexane/ethyl acetate to give almost pure compound 5xy.

Most of the final compound can be purified by crystallization easily, for those compounds which has good solubility, a short silica gel column purification is necessary.

Representative gram scale procedure for synthesis of 5

To a three necked 500 ml flask equipped with a thermometer was added 4lb (9.13 g, 20 mmol, 1 eq.), DMA (200 ml), anhydrous KOAc (azeotroped with toluene prior to use) (7.85 g, 80 mmol, 4 eq.), Pd(t-Bu3P)2 (511.05 mg, 1 mmol, 0.05 eq.). The mixture was heated under argon at 120 °C for 2 h. The mixture was diluted with H2O (30 ml) to precipitate the product, filtered and the solid was washed with H2O and ethanol successively. The crude product was dissolved in DCM/MeOH (5 : 1), filtered through celite to remove catalyst residue, then concentrated and re-crystallized from hexane/ethyl acetate to give pure compound 5lb (5.23 g, 19 mmol, 95% yield).

Phenanthridin-6(5H)-one (5aa)

Off-white solid, 129 mg, 66% yield, TLC Rf 0.5 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.69 (s, 1H), 8.52 (d, J = 8.0 Hz, 1H), 8.40 (d, J = 8.0 Hz, 1H), 8.33 (d, J = 7.6 Hz, 1H), 7.86 (t, J = 7.2 Hz, 1H), 7.65 (t, J = 7.4 Hz, 1H), 7.50 (t, J = 7.4 Hz, 1H), 7.38 (d, J = 8.0 Hz, 1H), 7.27 (t, J = 7.4 Hz, 1H). 13C NMR (100 MHz, DMSO-d6): δ 160.8, 136.5, 134.2, 132.8, 129.6, 127.9, 127.5, 125.7, 123.2, 122.6, 122.3, 117.5, 116.1. ESI-HRMS: calculated for C13H9NNaO [M + Na]+ 218.0576, found 218.0576.

2-Methoxyphenanthridin-6(5H)-one (5ab)

Off-white solid, 198 mg, 88% yield, TLC Rf 0.3 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, CDCl3): δ 11.23 (s, 1H), 8.61 (d, J = 7.6 Hz, 1H), 8.26 (d, J = 8.0 Hz, 1H), 7.83–7.79 (m, 1H), 7.68–7.62 (m, 2H), 7.38 (d, J = 8.8 Hz, 1H), 7.14–7.11 (m, 1H), 3.93 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.3, 154.8, 134.1, 132.5, 130.7, 127.9, 127.5, 125.9, 123.0, 118.3, 117.7, 117.3, 106.2, 55.6; HRMS (ESI) m/z calcd for C14H11NNaO2 [M + Na]+ 248.0682, found 248.0690.

3-Isopropylphenanthridin-6(5H)-one (5ae-a)

Off-white solid, 123 mg 52% yield, TLC Rf 0.5 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.60 (s, 1H), 8.46 (d, J = 8.0 Hz, 1H), 8.31–8.29 (m, 2H), 7.83 (t, J = 7.6 Hz, 1H), 7.61 (t, J = 7.4 Hz, 1H), 7.23 (s, 1H), 7.17 (d, J = 8.4 Hz, 1H), 2.93–3.00 (m, 1H), 1.25 (d, J = 6.8 Hz, 6H); 13C NMR (100 MHz, DMSO-d6): δ 160.9, 150.2, 136.6, 134.3, 132.7, 127.4, 125.3, 123.2, 122.4, 120.9, 115.6, 113.4, 33.3, 23.6; HRMS (ESI) m/z calcd for C16H15NNaO [M + Na]+ 260.1046, found 260.1033.

1-Isopropylphenanthridin-6(5H)-one (5ae-b)

Off-white solid, 62 mg, 26% yield, TLC Rf 0.5 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, CDCl3): δ 10.37 (s, 1H), 8.56 (d, J = 7.6 Hz, 1H), 8.24 (d, J = 8.0 Hz, 1H), 7.71 (t, J = 7.6 Hz, 1H), 7.55 (t, J = 6.8 Hz, 1H), 7.38 (t, J = 7.8 Hz, 1H), 7.28 (d, J = 7.6 Hz, 1H), 7.11 (d, J = 7.6 Hz, 1H), 3.98–3.93 (m, 1H), 1.39 (d, J = 6.8 Hz, 6H); 13C NMR (100 MHz, DMSO-d6): δ 160.4, 147.0, 137.2, 134.4, 131.9, 128.8, 127.6, 127.2, 127.0, 121.0, 116.1, 113.8, 30.0, 24.5; HRMS (ESI) m/z calcd for C16H15NNaO [M + Na]+ 260.1046, found 260.1046.

Thieno[3,2-c]isoquinolin-5(4H)-one (5af)

Off-white solid, 169 mg, 84% yield, TLC Rf 0.5 (20 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 12.01 (s, 1H), 8.27 (d, J = 7.6 Hz, 1H), 7.79–7.75 (m, 3H), 7.54–7.50 (m, 1H), 7.06 (d, J = 5.2 Hz, 1H); 13C NMR (100 MHz, DMSO-d6): δ 161.4, 138.4, 133.1, 133.0, 128.2, 127.7, 126.3, 123.6, 122.4, 117.9, 115.0; HRMS (ESI) m/z calcd for C11H7NNaOS [M + Na]+ 224.0141, found 224.0137.

3-tert-Butylphenanthridin-6(5H)-one (5aj)

Off-white solid, 206 mg, 82% yield, TLC Rf 0.7 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, CDCl3): δ 10.99 (s, 1H), 8.51 (d, J = 8.0 Hz, 1H), 8.20 (d, J = 8.0 Hz, 1H), 8.17 (d, J = 8.4 Hz, 1H), 7.74–7.69 (m, 1H), 7.54–7.50 (m, 1H), 7.33–7.27 (m, 2H), 1.35 (s, 9H); 13C NMR (100 MHz, CDCl3): δ 163.4, 153.3, 136.0, 135.0, 132.8, 128.2, 127.4, 125.5, 122.6, 121.9, 120.7, 116.2, 113.4, 35.0, 31.2; HRMS (ESI) m/z calcd for C17H18NO [M + H]+ 252.1383, found 252.1395.

6-Oxo-5,6-dihydrophenanthridine-2-carbonitrile (5ci)

Brow solid, 88 mg, 40% yield, TLC Rf 0.4 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 12.07 (s, 1H), 8.98 (d, J = 1.6 Hz, 1H), 8.65 (d, J = 8.0 Hz, 1H), 8.34–8.32 (m, 1H), 7.93–7.88 (m, 2H), 7.75–7.71 (m, 1H), 7.48 (d, J = 8.4 Hz, 1H); 13C NMR (100 MHz, DMSO-d6): δ 160.9, 139.7, 133.2, 132.9, 132.4, 129.0, 128.6, 127.4, 125.7, 123.2, 119.1, 118.2, 117.1, 104.5; HRMS (ESI) m/z calcd for C14H8N2NaO [M + Na]+ 243.0529, found 243.0516.

2-Methoxy-10-methylphenanthridin-6(5H)-one (5db)

Grey white solid, 194 mg, 81% yield, TLC Rf 0.4 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.59 (s, 1H), 8.32 (d, J = 7.6 Hz, 1H), 7.94 (d, J = 1.6 Hz, 1H), 7.71 (d, J = 7.6 Hz, 1H), 7.55 (t, J = 7.8 Hz, 1H), 7.36 (d, J = 8.8 Hz, 1H), 7.19–7.16 (m, 1H), 3.85 (s, 3H), 2.97 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.4, 153.8, 136.9, 135.1, 133.0, 131.0, 127.5, 127.3, 126.1, 119.4, 117.1, 116.1, 111.3, 55.3, 25.4; HRMS (ESI) m/z calcd for C15H13NNaO2 [M + Na]+ 262.0838, found 262.0842.

2-Methoxy-4,10-dimethylphenanthridin-6(5H)-one (5dc)

Off white solid, 220 mg, 87% yield, TLC Rf 0.7 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 8.77 (s, 1H), 8.51 (d, J = 7.6 Hz, 1H), 7.86 (s, 1H), 7.63 (d, J = 6.8 Hz, 1H), 7.50 (t, J = 7.6 Hz, 1H), 6.98 (s, 1H), 3.89 (s, 3H), 2.99 (s, 3H), 2.51 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.9, 153.2, 137.1, 135.1, 133.6, 129.2, 127.4, 127.3, 126.1, 125.2, 119.5, 117.6, 109.2, 55.3, 25.6, 18.2; HRMS (ESI) m/z calcd for C16H15NNaO2 [M + Na]+ 276.0995, found 276.1007.

9-Methylthieno[3,2-c]isoquinolin-5(4H)-one (5df)

Brown solid, 153 mg, 71% yield, TLC Rf 0.7 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 12.10 (s, 1H), 8.25 (d, J = 8.0 Hz, 1H), 7.90 (d, J = 5.2 Hz, 1H), 7.68 (d, J = 7.2 Hz, 1H), 7.44 (t, J = 7.6 Hz, 1H), 7.15 (d, J = 5.6 Hz, 1H), 2.75 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 161.3, 138.2, 134.7, 132.6, 132.1, 128.6, 126.3, 125.6, 124.6, 117.2, 113.9, 22.0; HRMS (ESI) m/z calcd for C12H9NNaOS [M + Na]+ 238.0297, found 238.0318.

2,7-Dimethoxy-4-methylphenanthridin-6(5H)-one (5ec)

Off-white solid, 247 mg, 92% yield, TLC Rf 0.7 (20 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 10.08 (s, 1H), 8.06 (d, J = 8.0 Hz, 1H), 7.73 (t, J = 8.2 Hz, 1H), 7.63 (d, J = 2.4 Hz, 1H), 7.18 (d, J = 8.4 Hz, 1H), 6.99 (d, J = 2.0 Hz, 1H), 3.89 (s, 3H), 3.84 (s, 3H), 2.42 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.9, 159.3, 153.9, 137.2, 133.4, 129.7, 125.0, 119.2, 117.8, 114.9, 114.7, 110.8, 104.4, 56.0, 55.5, 17.5; HRMS (ESI) m/z calcd for C16H16NO3 [M + H]+ 270.1125, found 270.1118.

6-Methoxythieno[3,2-c]isoquinolin-5(4H)-one (5ef)

Brown solid, 141 mg, 61% yield, TLC Rf 0.7 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 11.63 (s, 1H), 7.73 (d, J = 5.2 Hz, 1H), 7.65 (t, J = 8.2 Hz, 1H), 7.25 (d, J = 8.0 Hz, 1H), 7.03 (d, J = 8.4 Hz, 1H), 6.96 (d, J = 5.2 Hz, 1H). 3.86 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 161.3, 160.2, 138.9, 135.6, 134.0, 127.9, 117.5, 114.6, 114.3, 112.5, 108.9, 55.8; HRMS (ESI) m/z calcd for C12H9NNaO2S [M + Na]+ 254.0246, found 254.0257.

8-Methoxythieno[3,4-c]quinolin-4(5H)-one (5fb)

Brown solid, 143 mg, 62% yield, TLC Rf 0.6 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 11.06 (s, 1H), 8.49–8.47 (m, 2H), 7.66 (d, J = 2.8 Hz, 1H), 7.22 (d, J = 8.8 Hz, 1H), 7.03–7.00 (m, 1H), 3.84 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 157.7, 154.7, 136.3, 130.9, 130.2, 129.9, 119.6, 117.3, 117.2, 116.1, 107.5, 55.6; HRMS (ESI) m/z calcd for C12H9NNaO2S [M + Na]+ 254.0246, found 254.0246.

8-Methoxy-6-methylthieno[3,4-c]quinolin-4(5H)-one (5fc)

Brown solid, 142 mg, 58% yield, TLC Rf 0.7 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 10.08 (s, 1H), 8.52 (d, J = 2.0 Hz, 1H), 8.47 (s, 1H), 7.52 (s, 1H), 6.89 (s, 1H), 3.82 (s, 3H), 2.40 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 158.1, 154.3, 136.6, 130.7, 130.0, 128.5, 125.8, 119.7, 117.5, 117.3, 105.3, 55.4, 17.9; HRMS (ESI) m/z calcd for C13H11NNaO2S [M + Na]+ 268.0403, found 268.0398.

4-Chloro-7-fluoro-2-methoxyphenanthridin-6(5H)-one (5hd)

Light grey solid, 247 mg, 89% yield, TLC Rf 0.5 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 10.50 (s, 1H), 8.43 (d, J = 8.0 Hz, 1H), 7.89–7.85 (m, 2H), 7.45 (dd, J = 11.6, 8.4 Hz, 1H), 7.36 (d, J = 2.0 Hz, 1H); 3.89 (s. 3H); 13C NMR was not obtained due to low solubility; HRMS (ESI) m/z calcd for C14H9ClFNNaO2 [M + Na]+ 300.0198, found 300.0208.

Dithieno[3,2-b:3′,2′-d]pyridin-5(4H)-one (5if)

Brown solid, 176 mg, 85% yield, TLC Rf 0.6 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 12.23 (s, 1H), 8.17 (d, J = 4.0 Hz, 1H), 7.79 (d, J = 4.8 Hz, 1H), 7.61 (d, J = 4.4 Hz, 1H), 7.11 (d, J = 4.4 Hz, 1H); 13C NMR (100 MHz, DMSO-d6): δ 156.0, 139.9, 135.3, 127.5, 127.1, 122.6, 117.4, 113.3; HRMS (ESI) m/z calcd for C9H5NNaOS2 [M + Na]+ 229.9705, found 229.9718.

8-Methyl-6-oxo-5,6-dihydrophenanthridine-4-carbonitrile (5jh)

Brown solid, 87 mg, 37% yield, TLC Rf 0.6 (20 : 1, DCM : MeOH); 1H NMR (400 MHz, CDCl3): δ 8.93 (s, 1H), 8.42 (d, J = 8.0 Hz, 1H), 8.36 (s, 1H), 8.18 (d, J = 8.0 Hz, 1H), 7.75–7.68 (m, 2H), 7.36 (t, J = 7.8 Hz, 1H), 2.57 (s, 3H); 13C NMR was not obtained due to low solubility; HRMS (ESI) m/z calcd for C15H10N2NaO [M + Na]+ 257.0685, found 257.0696.

8-Methoxy-6-methylthieno[3,2-c]quinolin-4(5H)-one (5kc)

Brown solid, 204 mg, 83% yield, TLC Rf 0.7 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 10.73 (s, 1H), 7.78 (d, J = 5.6 Hz, 1H), 7.60 (d, J = 5.2 Hz, 1H), 7.11 (d, J = 2.4 Hz, 1H), 7.01 (d, J = 2.0 Hz, 1H), 3.83 (s, 3H), 2.46 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 158.1, 154.1, 145.8, 131.1, 129.0, 126.7, 126.4, 125.3, 119.3, 116.8, 103.1, 55.4, 17.8; HRMS (ESI) m/z calcd for C13H11NNaO2S [M + Na]+ 268.0403, found 268.0411.

Dithieno[3,2-b:2′,3′-d]pyridin-5(4H)-one (5kf)

Brown solid, 174 mg, 84% yield, TLC Rf 0.6 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 12.15 (s, 1H), 7.79 (d, J = 5.2 Hz, 1H), 7.62 (d, J = 5.2 Hz, 1H), 7.54 (d, J = 4.8 Hz, 1H), 7.09 (d, J = 5.2 Hz, 1H); 13C NMR (100 MHz, DMSO-d6): δ 158.4, 142.1, 139.4, 128.5, 127.6, 125.3, 124.1, 117.6, 112.2; HRMS (ESI) m/z calcd for C9H6NOS2 [M + H]+ 207.9885, found 207.9880.

6-Chlorothieno[3,2-c]quinolin-4(5H)-one (5kg)

Brown solid, 167 mg, 71% yield, TLC Rf 0.6 (20 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 10.91 (s, 1H), 7.88–7.86 (m, 2H), 7.66–7.63 (m, 2H), 7.27 (t, J = 7.8 Hz, 1H). 13C NMR (100 MHz, DMSO-d6): δ 157.9, 145.3, 132.5, 131.5, 129.4, 128.0, 125.3, 123.1, 122.6, 119.3, 117.9. ESI-HRMS: calculated for C11H6ClNNaOS [M + Na]+ 257.9751, found 257.9739.

2-Methoxybenzo[k]phenanthridin-6(5H)-one (5lb)

Off-white solid, 250 mg, 91% yield, TLC Rf 0.5 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.85 (s, 1H), 9.01 (d, J = 7.2 Hz, 1H), 8.33 (d, J = 8.8 Hz, 1H), 8.17–8.08 (m, 3H), 7.80–7.78 (m, 2H), 7.47 (d, J = 8.8 Hz, 1H), 7.28–7.25 (m, 1H), 3.90 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.4, 154.2, 135.7, 132.5, 131.5, 129.0, 128.6, 128.4, 128.1, 127.4, 126.9, 124.9, 122.9, 118.1, 117.4, 117.2, 111.1, 55.5; HRMS (ESI) m/z calcd for C18H14NO2 [M + H]+ 276.1019, found 276.1028.

Benzo[f]thieno[3,2-c]isoquinolin-5(4H)-one (5lf)

Brown solid, 229 mg, 91% yield, TLC Rf 0.7 (20 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 12.55 (s, 1H), 8.89 (d, J = 8.4 Hz, 1H), 8.39 (d, J = 8.8 Hz, 1H), 8.17 (d, J = 7.6 Hz, 1H), 8.04–8.01 (m, 2H), 7.90 (t, J = 7.4 Hz, 1H), 7.83 (t, J = 7.4 Hz, 1H), 7.26 (d, J = 5.6 Hz, 1H); 13C NMR (100 MHz, DMSO-d6): δ 161.2, 140.1, 135.1, 131.8, 129.4, 129.2, 128.4, 127.6, 127.1, 126.8, 125.5, 124.1, 122.1, 117.4, 112.8; HRMS (ESI) m/z calcd for C15H9NNaO [M + Na]+ 274.0297, found 274.0314.

4-Chlorobenzo[k]phenanthridin-6(5H)-one (5lg)

Grey solid, 210 mg, 75% yield, TLC Rf 0.4 (2 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.08 (s, 1H), 8.89–8.87 (m, 1H), 8.58 (d, J = 8.0 Hz, 1H), 8.33 (d, J = 8.4 Hz, 1H), 8.20–8.15 (m, 2H), 7.83–7.74 (m, 3H), 7.38 (t, J = 8.0 Hz, 1H); 13C NMR (100 MHz, DMSO-d6): δ 156.2, 131.3, 128.2, 127.7, 124.3, 123.9, 123.7, 123.1, 122.2, 122.0, 121.9, 119.6, 118.0, 117.0, 115.1, 114.9, 113.6; HRMS (ESI) m/z calcd for C17H11ClNO [M + H]+ 276.1019, found 276.1026.

2,8-Dimethoxyphenanthridin-6(5H)-one (5mb)

Light yellow solid, 174 mg, 68% yield, TLC Rf 0.4 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.58 (s, 1H), 8.49 (d, J = 9.2 Hz, 1H), 7.80–7.76 (m, 2H), 7.45–7.42 (m, 1H), 7.28 (d, J = 8.8 Hz, 1H), 7.08 (dd, J = 8.8, 2.8 Hz, 1H), 3.92 (s, 3H), 3.86 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.1, 159.0, 154.9, 129.6, 127.5, 127.3, 124.9, 121.3, 118.5, 117.1, 116.5, 108.7, 105.7, 55.6, 55.4; HRMS (ESI) m/z calcd for C15H13NNaO3 [M + Na]+ 278.0788, found 278.0797.

2,8-Dimethoxy-4-methylphenanthridin-6(5H)-one (5mc)

Light yellow solid, 180 mg, 67% yield, TLC Rf 0.5 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, CDCl3): δ 8.66 (s, 1H), 8.08 (d, J = 8.8 Hz, 1H), 7.86 (d, J = 2.8 Hz, 1H), 7.40 (d, J = 2.4 Hz, 1H), 7.31 (dd, J = 8.8, 2.8 Hz, 1H), 6.84 (d, J = 2.0 Hz, 1H), 3.90 (s, 3H), 3.83 (s, 3H), 2.40 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 160.5, 159.0, 154.3, 128.0, 127.8, 127.0, 125.7, 125.2, 121.7, 118.5, 117.9, 108.4, 103.5, 55.5, 17.7; HRMS (ESI) m/z calcd for C16H15NNaO3 [M + Na]+ 292.0944, found 292.0954.

2-Isopropyl-8-methoxyphenanthridin-6(5H)-one (5mk)

Off-white solid, 120 mg, 45% yield, TLC Rf 0.6 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, CDCl3): δ 11.16 (s, 1H), 8.27 (d, J = 9.2 Hz, 1H), 8.03 (d, J = 2.0 Hz, 1H), 7.99 (s, 1H), 7.42–7.35 (m, 3H), 4.02 (s, 3H), 3.10–3.03 (m, 1H), 1.36 (d, J = 6.8 Hz, 6H); 13C NMR (100 MHz, CDCl3): δ 159.3, 143.5, 133.1, 128.6, 127.0, 123.8, 122.6, 119.6, 118.5, 116.7, 108.7, 55.7, 34.1, 24.3; HRMS (ESI) m/z calcd for C17H17NNaO2 [M + Na]+ 290.1151, found 290.1147.

3-tert-Butyl-10-methylphenanthridin-6(5H)-one (5nj)

Off-white solid, 207 mg, 78% yield, TLC Rf 0.7 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.58 (s, 1H), 8.39 (d, J = 8.8 Hz, 1H), 8.29 (d, J = 7.2 Hz, 1H), 7.69 (d, J = 7.2 Hz, 1H), 7.51 (t, J = 7.6 Hz, 1H), 7.45 (d, J = 1.6 Hz, 1H), 7.32 (dd, J = 8.8, 2.0 Hz, 1H), 2.92 (s, 3H), 1.34 (s, 9H); 13C NMR (100 MHz, DMSO-d6): δ 161.0, 151.5, 136.9, 136.8, 134.9, 133.2, 127.1, 126.8, 126.0, 119.3, 116.4, 112.7, 34.4, 30.8, 25.5; HRMS (ESI) m/z calcd for C18H19NNaO [M + Na]+ 288.1359, found 288.1370.

8-Methoxythieno[3,2-c]quinolin-4(5H)-one (5ob)

Brown solid, 123 mg, 53% yield, TLC Rf 0.7 (10 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 11.63 (s, 1H), 7.79 (d, J = 5.2 Hz, 1H), 7.58 (d, J = 5.2 Hz, 1H), 7.36 (d, J = 8.8 Hz, 1H), 7.26 (d, J = 2.4 Hz, 1H), 7.14 (dd, J = 8.8, 2.8 Hz, 1H), 3.85 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 157.7, 154.6, 145.1, 131.4, 130.4, 126.7, 125.3, 118.2, 117.6, 116.8, 105.2, 55.6; HRMS (ESI) m/z calcd for C12H9NNaO2S [M + Na]+ 254.0246, found 254.0252.

8-Isopropylthieno[3,2-c]quinolin-4(5H)-one (5ok)

Brown solid, 124 mg, 51% yield, TLC Rf 0.5 (20 : 1, DCM : MeOH); 1H NMR (400 MHz, DMSO-d6): δ 11.67 (s, 1H), 7.77 (d, J = 5.2 Hz, 1H), 7.63 (d, J = 2.8 Hz, 1H), 7.58 (d, J = 5.2 Hz, 1H), 7.42–7.35 (m, 2H), 3.04–2.97 (m, 1H), 1.26 (d, J = 6.8 Hz, 6H); 13C NMR (100 MHz, DMSO-d6): δ 158.1, 145.6, 142.7, 134.4, 131.1, 127.9, 126.4, 125.3, 120.3, 116.3, 116.1, 32.9, 23.9; HRMS (ESI) m/z calcd for C14H13NNaOS [M + Na]+ 266.0610, found 266.0641.

4-Fluoro-7-methoxyphenanthridin-6(5H)-one (5pl)

Light yellow solid, 93 mg, 38% yield, TLC Rf 0.5 (1 : 1, petroleum ether : EtOAc); 1H NMR (400 MHz, DMSO-d6): δ 11.12 (s, 1H), 8.14 (d, J = 8.0 Hz, 1H), 8.04 (d, J = 8.0 Hz, 1H), 7.78 (t, J = 8.2 Hz, 1H), 7.38–7.34 (m, 1H), 7.24 (d, J = 8.4 Hz, 1H), 7.20–7.15 (m, 1H), 3.90 (s, 3H); 13C NMR (100 MHz, DMSO-d6): δ 161.0, 159.0, 150.0, 147.6, 136.4, 133.9, 125.8, 125.7, 121.4, 121.3, 119.5, 114.9, 114.8, 114.7, 111.5, 56.0; HRMS (ESI) m/z calcd for C14H10FNNaO2 [M + Na]+ 266.0588, found 266.0599.

Conflicts of interest

There are no conflicts of interest to declare.