Crystal structure of methyl 1-methyl-2-oxo-spiro-[indoline-3,2'-oxirane]-3'-carboxyl-ate.

In the title compound, C12H11NO4, the dihedral angle between the indole ring system (r.m.s. deviation = 0.019 Å) and the oxirane ring is 88.8 (2)°. The oxirane O atom and the bridging ester O atom are in an approximate syn conformation [O-C-C-O = -25.4 (3)°] In the crystal, inversion dimers linked by pair of C-H⋯O hydrogen bonds generate R 2 (2)(8) loops, where the C-H donor group forms part of the oxirane ring. A second C-H⋯O inter-action arising from one of the C-H groups of the benzene ring links the dimers into [001] double chains.

Related literature

For the bioactivity of indole derivatives, see: Di Fabio et al. (2007 ▸); Sharma & Tepe (2004 ▸). For a related structure, see: Savithri et al. (2015 ▸).

Experimental

Crystal data

C12H11NO4

M = 233.22

Triclinic,

a = 7.1401 (4) Å

b = 8.7787 (4) Å

c = 9.0678 (4) Å

α = 91.517 (3)°

β = 104.227 (3)°

γ = 94.714 (3)°

V = 548.44 (5) Å3

Z = 2

Mo Kα radiation

μ = 0.11 mm−1

T = 293 K

0.35 × 0.30 × 0.30 mm

Data collection

Bruker Kappa APEXII CCD diffractometer

Absorption correction: multi-scan (SADABS; Bruker, 2004 ▸) T min = 0.963, T max = 0.969

11311 measured reflections

1927 independent reflections

1480 reflections with I > 2σ(I)

R int = 0.037

Refinement

R[F 2 > 2σ(F 2)] = 0.055

wR(F 2) = 0.173

S = 1.06

1927 reflections

158 parameters

H atoms treated by a mixture of independent and constrained refinement

Δρmax = 0.30 e Å−3

Δρmin = −0.27 e Å−3

Data collection: APEX2 (Bruker, 2004 ▸); cell refinement: SAINT (Bruker, 2004 ▸); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▸); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▸); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012 ▸); software used to prepare material for publication: SHELXL97 and PLATON (Spek, 2009 ▸).

Crystal structure: contains datablock(s) global, I. DOI: 10.1107/S2056989015006398/hb7369sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989015006398/hb7369Isup2.hkl

Click here for additional data file.

Supporting information file. DOI: 10.1107/S2056989015006398/hb7369Isup3.cml

Click here for additional data file.

. DOI: 10.1107/S2056989015006398/hb7369fig1.tif

The mol­ecular structure of the title compound with displacement ellipsoids drawn at the 30% probability level.

Click here for additional data file.

a . DOI: 10.1107/S2056989015006398/hb7369fig2.tif

The mol­ecular packing as viewed along the a axis. Dashed lines shows the C—H⋯O hydrogen bonds. H atoms not involved in hydrogen bonding have been omitted for clarity.

Click here for additional data file.

a . DOI: 10.1107/S2056989015006398/hb7369fig3.tif

A partial view of the hydrogen-bond inter­actions C9—H9⋯O1 and C3—H3⋯O3 along a axis.

CCDC reference: 1056692

Additional supporting information: crystallographic information; 3D view; checkCIF report

C12H11NO4	Z = 2
Mr = 233.22	F(000) = 244
Triclinic, P1	Dx = 1.412 Mg m−3
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 7.1401 (4) Å	Cell parameters from 1927 reflections
b = 8.7787 (4) Å	θ = 2.3–25.0°
c = 9.0678 (4) Å	µ = 0.11 mm−1
α = 91.517 (3)°	T = 293 K
β = 104.227 (3)°	Block, colourless
γ = 94.714 (3)°	0.35 × 0.30 × 0.30 mm
V = 548.44 (5) Å3

Bruker Kappa APEXII CCD diffractometer	1927 independent reflections
Radiation source: fine-focus sealed tube	1480 reflections with I > 2σ(I)
Graphite monochromator	Rint = 0.037
ω and φ scans	θmax = 25.0°, θmin = 2.3°
Absorption correction: multi-scan (SADABS; Bruker, 2004)	h = −8→8
Tmin = 0.963, Tmax = 0.969	k = −10→10
11311 measured reflections	l = −10→10

Refinement on F2	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.055	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.173	H atoms treated by a mixture of independent and constrained refinement
S = 1.06	w = 1/[σ2(Fo2) + (0.102P)2 + 0.172P] where P = (Fo2 + 2Fc2)/3
1927 reflections	(Δ/σ)max < 0.001
158 parameters	Δρmax = 0.30 e Å−3
0 restraints	Δρmin = −0.27 e Å−3

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > 2sigma(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

	x	y	z	Uiso*/Ueq
O2	0.0254 (2)	0.10821 (18)	0.36778 (18)	0.0462 (5)
O4	0.1745 (3)	−0.03538 (19)	0.15149 (19)	0.0536 (5)
O3	0.4764 (3)	0.0432 (2)	0.2809 (2)	0.0632 (6)
O1	0.1739 (3)	0.3246 (2)	0.1663 (2)	0.0643 (6)
N1	0.2372 (3)	0.4866 (2)	0.3794 (3)	0.0504 (6)
C7	0.2040 (3)	0.3195 (3)	0.5623 (3)	0.0425 (6)
C2	0.3047 (4)	0.0282 (2)	0.2698 (3)	0.0429 (6)
C4	0.1736 (3)	0.2320 (2)	0.4166 (2)	0.0379 (5)
C3	0.2223 (4)	0.0750 (3)	0.3974 (3)	0.0428 (6)
C6	0.2456 (3)	0.4711 (3)	0.5343 (3)	0.0486 (6)
C5	0.1928 (3)	0.3492 (3)	0.3012 (3)	0.0438 (6)
C8	0.2075 (4)	0.2738 (4)	0.7065 (3)	0.0566 (7)
H8	0.1811	0.1715	0.7247	0.068*
C11	0.2901 (4)	0.5825 (4)	0.6509 (4)	0.0717 (10)
H11	0.3174	0.6849	0.6334	0.086*
C1	0.2456 (5)	−0.0803 (4)	0.0221 (3)	0.0692 (9)
H1A	0.1393	−0.1255	−0.0577	0.104*
H1B	0.3391	−0.1534	0.0521	0.104*
H1C	0.3056	0.0081	−0.0141	0.104*
C12	0.2681 (5)	0.6277 (3)	0.3066 (5)	0.0774 (10)
H12A	0.2979	0.7114	0.3813	0.116*
H12B	0.1528	0.6440	0.2303	0.116*
H12C	0.3742	0.6214	0.2597	0.116*
C10	0.2921 (5)	0.5344 (5)	0.7951 (4)	0.0845 (12)
H10	0.3223	0.6068	0.8761	0.101*
C9	0.2516 (5)	0.3848 (5)	0.8237 (4)	0.0796 (11)
H9	0.2537	0.3576	0.9225	0.096*
H3	0.273 (4)	0.024 (3)	0.488 (3)	0.052 (7)*

	U11	U22	U33	U12	U13	U23
O2	0.0454 (10)	0.0440 (9)	0.0450 (9)	−0.0086 (7)	0.0076 (7)	0.0005 (7)
O4	0.0565 (11)	0.0523 (11)	0.0456 (10)	0.0033 (8)	0.0026 (8)	−0.0115 (8)
O3	0.0524 (13)	0.0730 (13)	0.0597 (12)	0.0065 (9)	0.0068 (9)	−0.0112 (9)
O1	0.0859 (15)	0.0673 (12)	0.0455 (11)	0.0096 (10)	0.0247 (10)	0.0167 (9)
N1	0.0464 (12)	0.0339 (11)	0.0738 (15)	0.0021 (8)	0.0206 (10)	0.0087 (9)
C7	0.0352 (12)	0.0495 (14)	0.0418 (13)	0.0004 (10)	0.0099 (9)	−0.0061 (10)
C2	0.0477 (15)	0.0335 (12)	0.0425 (13)	0.0041 (10)	0.0020 (10)	0.0010 (9)
C4	0.0380 (12)	0.0387 (12)	0.0351 (11)	−0.0034 (9)	0.0078 (9)	0.0011 (9)
C3	0.0477 (14)	0.0373 (12)	0.0382 (13)	−0.0010 (10)	0.0024 (10)	0.0032 (10)
C6	0.0333 (13)	0.0470 (14)	0.0650 (17)	0.0033 (10)	0.0125 (11)	−0.0104 (11)
C5	0.0425 (13)	0.0441 (13)	0.0476 (14)	0.0047 (10)	0.0154 (10)	0.0087 (10)
C8	0.0495 (15)	0.0805 (19)	0.0392 (14)	−0.0009 (13)	0.0128 (11)	−0.0032 (12)
C11	0.0491 (17)	0.0595 (18)	0.100 (3)	0.0038 (13)	0.0116 (16)	−0.0328 (17)
C1	0.077 (2)	0.082 (2)	0.0455 (15)	0.0188 (16)	0.0083 (13)	−0.0170 (14)
C12	0.0574 (18)	0.0453 (16)	0.137 (3)	0.0067 (13)	0.0348 (18)	0.0312 (17)
C10	0.061 (2)	0.110 (3)	0.074 (2)	0.0127 (19)	0.0073 (16)	−0.052 (2)
C9	0.062 (2)	0.128 (3)	0.0476 (17)	0.0067 (19)	0.0138 (14)	−0.0251 (18)

O2—C3	1.421 (3)	C3—H3	0.95 (3)
O2—C4	1.433 (3)	C6—C11	1.380 (4)
O4—C2	1.311 (3)	C8—C9	1.382 (4)
O4—C1	1.446 (3)	C8—H8	0.9300
O3—C2	1.201 (3)	C11—C10	1.382 (5)
O1—C5	1.209 (3)	C11—H11	0.9300
N1—C5	1.356 (3)	C1—H1A	0.9600
N1—C6	1.402 (3)	C1—H1B	0.9600
N1—C12	1.446 (3)	C1—H1C	0.9600
C7—C8	1.373 (3)	C12—H12A	0.9600
C7—C6	1.384 (4)	C12—H12B	0.9600
C7—C4	1.470 (3)	C12—H12C	0.9600
C2—C3	1.484 (4)	C10—C9	1.367 (5)
C4—C3	1.466 (3)	C10—H10	0.9300
C4—C5	1.509 (3)	C9—H9	0.9300
C3—O2—C4	61.80 (14)	O1—C5—C4	126.6 (2)
C2—O4—C1	116.2 (2)	N1—C5—C4	106.3 (2)
C5—N1—C6	111.2 (2)	C7—C8—C9	117.8 (3)
C5—N1—C12	122.4 (3)	C7—C8—H8	121.1
C6—N1—C12	126.4 (2)	C9—C8—H8	121.1
C8—C7—C6	121.6 (2)	C6—C11—C10	116.7 (3)
C8—C7—C4	131.6 (2)	C6—C11—H11	121.7
C6—C7—C4	106.7 (2)	C10—C11—H11	121.7
O3—C2—O4	125.0 (2)	O4—C1—H1A	109.5
O3—C2—C3	121.3 (2)	O4—C1—H1B	109.5
O4—C2—C3	113.7 (2)	H1A—C1—H1B	109.5
O2—C4—C3	58.71 (14)	O4—C1—H1C	109.5
O2—C4—C7	123.07 (19)	H1A—C1—H1C	109.5
C3—C4—C7	125.9 (2)	H1B—C1—H1C	109.5
O2—C4—C5	116.78 (18)	N1—C12—H12A	109.5
C3—C4—C5	121.0 (2)	N1—C12—H12B	109.5
C7—C4—C5	105.51 (19)	H12A—C12—H12B	109.5
O2—C3—C4	59.48 (14)	N1—C12—H12C	109.5
O2—C3—C2	119.95 (19)	H12A—C12—H12C	109.5
C4—C3—C2	121.3 (2)	H12B—C12—H12C	109.5
O2—C3—H3	117.1 (15)	C9—C10—C11	122.8 (3)
C4—C3—H3	116.4 (16)	C9—C10—H10	118.6
C2—C3—H3	112.8 (15)	C11—C10—H10	118.6
C11—C6—C7	120.9 (3)	C10—C9—C8	120.3 (3)
C11—C6—N1	128.8 (3)	C10—C9—H9	119.9
C7—C6—N1	110.3 (2)	C8—C9—H9	119.9
O1—C5—N1	127.2 (2)
C1—O4—C2—O3	−4.4 (4)	C4—C7—C6—N1	2.0 (3)
C1—O4—C2—C3	178.6 (2)	C5—N1—C6—C11	178.4 (2)
C3—O2—C4—C7	−115.0 (2)	C12—N1—C6—C11	−2.3 (4)
C3—O2—C4—C5	111.7 (2)	C5—N1—C6—C7	−0.6 (3)
C8—C7—C4—O2	44.0 (4)	C12—N1—C6—C7	178.7 (2)
C6—C7—C4—O2	−140.1 (2)	C6—N1—C5—O1	179.6 (2)
C8—C7—C4—C3	−28.9 (4)	C12—N1—C5—O1	0.2 (4)
C6—C7—C4—C3	147.0 (2)	C6—N1—C5—C4	−1.0 (3)
C8—C7—C4—C5	−178.4 (2)	C12—N1—C5—C4	179.7 (2)
C6—C7—C4—C5	−2.5 (2)	O2—C4—C5—O1	−37.7 (3)
C4—O2—C3—C2	−110.9 (2)	C3—C4—C5—O1	30.3 (4)
C7—C4—C3—O2	110.4 (2)	C7—C4—C5—O1	−178.4 (2)
C5—C4—C3—O2	−104.4 (2)	O2—C4—C5—N1	142.9 (2)
O2—C4—C3—C2	108.6 (2)	C3—C4—C5—N1	−149.1 (2)
C7—C4—C3—C2	−141.0 (2)	C7—C4—C5—N1	2.2 (2)
C5—C4—C3—C2	4.2 (3)	C6—C7—C8—C9	0.9 (4)
O3—C2—C3—O2	157.5 (2)	C4—C7—C8—C9	176.2 (3)
O4—C2—C3—O2	−25.4 (3)	C7—C6—C11—C10	0.5 (4)
O3—C2—C3—C4	87.1 (3)	N1—C6—C11—C10	−178.5 (2)
O4—C2—C3—C4	−95.8 (2)	C6—C11—C10—C9	−0.3 (5)
C8—C7—C6—C11	−0.8 (4)	C11—C10—C9—C8	0.5 (5)
C4—C7—C6—C11	−177.1 (2)	C7—C8—C9—C10	−0.7 (4)
C8—C7—C6—N1	178.4 (2)

D—H···A	D—H	H···A	D···A	D—H···A
C3—H3···O3i	0.95 (3)	2.52 (3)	3.414 (3)	157 (2)
C9—H9···O1ii	0.93	2.43	3.335 (4)	163

Table 1

Hydrogen-bond geometry (, )

DHA	DH	HA	D A	DHA
C3H3O3i	0.95(3)	2.52(3)	3.414(3)	157(2)
C9H9O1ii	0.93	2.43	3.335(4)	163

Symmetry codes: (i) ; (ii) .