In the title compound, C
26H
24N
2O
3, the hydrogenated pyrrole ring adopts a twist conformation and the pyran ring adopts a twist–boat conformation. The molecular packing is stabilized by N—H
O and C—H
O intermolecular hydrogen bonds and also by weak intermolecular π–π interactions.
Supporting information
CCDC reference: 274345
Key indicators
- Single-crystal X-ray study
- T = 273 K
- Mean (C-C) = 0.002 Å
- R factor = 0.050
- wR factor = 0.162
- Data-to-parameter ratio = 17.3
checkCIF/PLATON results
No syntax errors found
Alert level C
PLAT029_ALERT_3_C _diffrn_measured_fraction_theta_full Low ....... 0.97
PLAT420_ALERT_2_C D-H Without Acceptor N2 - H2 ... ?
0 ALERT level A = In general: serious problem
0 ALERT level B = Potentially serious problem
2 ALERT level C = Check and explain
0 ALERT level G = General alerts; check
0 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
1 ALERT type 2 Indicator that the structure model may be wrong or deficient
1 ALERT type 3 Indicator that the structure quality may be low
0 ALERT type 4 Improvement, methodology, query or suggestion
Data collection: SMART (Bruker, 2001); cell refinement: SAINT (Bruker, 2001); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ORTEP-3 (Farrugia, 1997) and PLATON (Spek, 2003); software used to prepare material for publication: SHELXL97 and PARST (Nardelli, 1995).
Methyl 2-(1
H-indol-3-ylmethyl)-1,2,3,3a,4,11
c-
hexahydronaphtho[2',1':2,3]pyrano[4,5-
b]pyrrole-2-carboxylate
top
Crystal data top
C26H24N2O3 | F(000) = 872 |
Mr = 412.47 | Dx = 1.326 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: -P 2ybc | Cell parameters from 7163 reflections |
a = 8.7481 (8) Å | θ = 2.3–27.6° |
b = 19.0068 (18) Å | µ = 0.09 mm−1 |
c = 12.4940 (12) Å | T = 273 K |
β = 95.891 (2)° | Block, colourless |
V = 2066.4 (3) Å3 | 0.26 × 0.22 × 0.20 mm |
Z = 4 | |
Data collection top
CCD area-setector diffractometer | 3776 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.017 |
Graphite monochromator | θmax = 28.0°, θmin = 2.0° |
ω scans | h = −11→11 |
17613 measured reflections | k = −24→24 |
4839 independent reflections | l = −16→16 |
Refinement top
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)] = 0.050 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.162 | H-atom parameters constrained |
S = 1.01 | w = 1/[σ2(Fo2) + (0.1029P)2 + 0.2052P] where P = (Fo2 + 2Fc2)/3 |
4839 reflections | (Δ/σ)max < 0.001 |
280 parameters | Δρmax = 0.43 e Å−3 |
0 restraints | Δρmin = −0.34 e Å−3 |
Special details top
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes)
are estimated using the full covariance matrix. The cell e.s.d.'s are taken
into account individually in the estimation of e.s.d.'s in distances, angles
and torsion angles; correlations between e.s.d.'s in cell parameters are only
used when they are defined by crystal symmetry. An approximate (isotropic)
treatment of cell e.s.d.'s is used for estimating e.s.d.'s 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 >
σ(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. |
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top | x | y | z | Uiso*/Ueq | |
N1 | 0.33765 (17) | 0.63409 (8) | 0.45999 (12) | 0.0693 (4) | |
H1 | 0.4027 | 0.6488 | 0.5114 | 0.083* | |
N2 | 0.21157 (13) | 0.45131 (7) | 0.20799 (9) | 0.0546 (3) | |
H2 | 0.2979 | 0.4729 | 0.2074 | 0.065* | |
O1 | 0.18670 (17) | 0.27824 (6) | 0.05427 (10) | 0.0760 (4) | |
O2 | 0.37017 (12) | 0.39147 (7) | 0.38624 (9) | 0.0703 (3) | |
O3 | 0.17640 (13) | 0.41084 (7) | 0.48534 (8) | 0.0647 (3) | |
C1 | 0.30168 (18) | 0.66730 (8) | 0.36399 (13) | 0.0598 (4) | |
C2 | 0.3569 (2) | 0.73010 (9) | 0.32392 (17) | 0.0722 (5) | |
H2A | 0.4315 | 0.7567 | 0.3641 | 0.087* | |
C3 | 0.2970 (3) | 0.75098 (9) | 0.22344 (18) | 0.0843 (6) | |
H3 | 0.3317 | 0.7925 | 0.1949 | 0.101* | |
C4 | 0.1853 (3) | 0.71147 (10) | 0.16297 (17) | 0.0872 (6) | |
H4 | 0.1468 | 0.7272 | 0.0950 | 0.105* | |
C5 | 0.1306 (2) | 0.64953 (9) | 0.20191 (14) | 0.0701 (5) | |
H5 | 0.0557 | 0.6237 | 0.1609 | 0.084* | |
C6 | 0.18934 (17) | 0.62614 (8) | 0.30377 (12) | 0.0556 (4) | |
C7 | 0.16100 (16) | 0.56592 (8) | 0.36747 (12) | 0.0547 (4) | |
C8 | 0.2533 (2) | 0.57354 (10) | 0.46104 (14) | 0.0657 (4) | |
H8 | 0.2585 | 0.5419 | 0.5181 | 0.079* | |
C9 | 0.05195 (16) | 0.50689 (8) | 0.33601 (12) | 0.0563 (4) | |
H9A | −0.0204 | 0.5224 | 0.2767 | 0.068* | |
H9B | −0.0060 | 0.4964 | 0.3962 | 0.068* | |
C10 | 0.13025 (15) | 0.43893 (8) | 0.30244 (11) | 0.0508 (3) | |
C11 | 0.12102 (15) | 0.42066 (7) | 0.11408 (10) | 0.0475 (3) | |
H11 | 0.0427 | 0.4548 | 0.0867 | 0.057* | |
C12 | 0.04063 (17) | 0.35726 (8) | 0.15773 (12) | 0.0548 (3) | |
H12 | −0.0558 | 0.3474 | 0.1131 | 0.066* | |
C13 | 0.00873 (17) | 0.38030 (9) | 0.26965 (13) | 0.0607 (4) | |
H13A | 0.0205 | 0.3411 | 0.3196 | 0.073* | |
H13B | −0.0948 | 0.3988 | 0.2688 | 0.073* | |
C14 | 0.21714 (15) | 0.40259 (7) | 0.02486 (10) | 0.0478 (3) | |
C15 | 0.2411 (2) | 0.33382 (8) | −0.00062 (12) | 0.0580 (4) | |
C16 | 0.1463 (2) | 0.29465 (9) | 0.15989 (13) | 0.0677 (4) | |
H16A | 0.2389 | 0.3045 | 0.2071 | 0.081* | |
H16B | 0.0962 | 0.2543 | 0.1886 | 0.081* | |
C17 | 0.28022 (15) | 0.45626 (8) | −0.03766 (10) | 0.0475 (3) | |
C18 | 0.26839 (16) | 0.52844 (8) | −0.01322 (12) | 0.0533 (3) | |
H18 | 0.2183 | 0.5420 | 0.0456 | 0.064* | |
C19 | 0.32939 (17) | 0.57877 (9) | −0.07455 (14) | 0.0622 (4) | |
H19 | 0.3211 | 0.6260 | −0.0565 | 0.075* | |
C20 | 0.40379 (18) | 0.55997 (10) | −0.16377 (14) | 0.0654 (4) | |
H20 | 0.4415 | 0.5946 | −0.2066 | 0.078* | |
C21 | 0.42096 (17) | 0.49118 (10) | −0.18791 (12) | 0.0637 (4) | |
H21 | 0.4732 | 0.4791 | −0.2464 | 0.076* | |
C22 | 0.36145 (16) | 0.43757 (9) | −0.12633 (11) | 0.0552 (4) | |
C23 | 0.3822 (2) | 0.36534 (10) | −0.14775 (12) | 0.0666 (4) | |
H23 | 0.4365 | 0.3523 | −0.2048 | 0.080* | |
C24 | 0.3247 (2) | 0.31496 (10) | −0.08713 (13) | 0.0701 (5) | |
H24 | 0.3401 | 0.2677 | −0.1024 | 0.084* | |
C25 | 0.24170 (16) | 0.41158 (8) | 0.39420 (11) | 0.0528 (3) | |
C26 | 0.2679 (2) | 0.38595 (10) | 0.57986 (13) | 0.0744 (5) | |
H26A | 0.2087 | 0.3880 | 0.6404 | 0.112* | |
H26B | 0.3576 | 0.4150 | 0.5936 | 0.112* | |
H26C | 0.2986 | 0.3382 | 0.5688 | 0.112* | |
Atomic displacement parameters (Å2) top | U11 | U22 | U33 | U12 | U13 | U23 |
N1 | 0.0684 (9) | 0.0778 (9) | 0.0594 (8) | −0.0048 (7) | −0.0038 (6) | −0.0102 (7) |
N2 | 0.0456 (6) | 0.0773 (8) | 0.0418 (6) | −0.0142 (6) | 0.0092 (5) | −0.0108 (5) |
O1 | 0.1110 (10) | 0.0514 (6) | 0.0674 (7) | 0.0057 (6) | 0.0172 (7) | −0.0024 (5) |
O2 | 0.0523 (6) | 0.0989 (9) | 0.0592 (7) | 0.0136 (6) | 0.0023 (5) | −0.0082 (6) |
O3 | 0.0676 (7) | 0.0822 (8) | 0.0452 (5) | 0.0074 (5) | 0.0108 (5) | 0.0016 (5) |
C1 | 0.0589 (8) | 0.0598 (9) | 0.0615 (9) | 0.0113 (7) | 0.0100 (7) | −0.0110 (7) |
C2 | 0.0782 (11) | 0.0544 (9) | 0.0857 (12) | 0.0081 (8) | 0.0159 (9) | −0.0143 (8) |
C3 | 0.1174 (17) | 0.0477 (9) | 0.0901 (14) | 0.0165 (10) | 0.0212 (12) | 0.0002 (9) |
C4 | 0.1266 (18) | 0.0623 (10) | 0.0711 (12) | 0.0310 (11) | 0.0033 (11) | 0.0024 (9) |
C5 | 0.0849 (12) | 0.0612 (10) | 0.0622 (10) | 0.0217 (8) | −0.0016 (8) | −0.0068 (7) |
C6 | 0.0544 (8) | 0.0575 (8) | 0.0555 (8) | 0.0149 (6) | 0.0086 (6) | −0.0104 (6) |
C7 | 0.0477 (7) | 0.0666 (9) | 0.0505 (7) | 0.0068 (6) | 0.0092 (6) | −0.0076 (6) |
C8 | 0.0668 (10) | 0.0767 (11) | 0.0535 (8) | −0.0052 (8) | 0.0061 (7) | −0.0009 (7) |
C9 | 0.0436 (7) | 0.0738 (9) | 0.0523 (8) | 0.0036 (6) | 0.0088 (6) | −0.0027 (7) |
C10 | 0.0405 (6) | 0.0687 (9) | 0.0440 (7) | −0.0046 (6) | 0.0077 (5) | −0.0052 (6) |
C11 | 0.0437 (7) | 0.0534 (7) | 0.0443 (7) | 0.0028 (5) | −0.0006 (5) | −0.0035 (5) |
C12 | 0.0509 (7) | 0.0615 (8) | 0.0508 (8) | −0.0065 (6) | −0.0015 (6) | −0.0029 (6) |
C13 | 0.0473 (7) | 0.0775 (10) | 0.0577 (9) | −0.0128 (7) | 0.0069 (6) | −0.0049 (7) |
C14 | 0.0491 (7) | 0.0556 (8) | 0.0370 (6) | 0.0066 (6) | −0.0039 (5) | −0.0022 (5) |
C15 | 0.0700 (9) | 0.0559 (8) | 0.0469 (7) | 0.0071 (7) | 0.0000 (6) | −0.0030 (6) |
C16 | 0.0838 (11) | 0.0614 (9) | 0.0588 (9) | 0.0013 (8) | 0.0113 (8) | 0.0057 (7) |
C17 | 0.0414 (6) | 0.0616 (8) | 0.0377 (6) | 0.0060 (6) | −0.0051 (5) | 0.0001 (5) |
C18 | 0.0470 (7) | 0.0588 (8) | 0.0532 (8) | 0.0068 (6) | 0.0014 (6) | 0.0031 (6) |
C19 | 0.0479 (7) | 0.0640 (9) | 0.0729 (10) | 0.0045 (6) | −0.0020 (7) | 0.0115 (8) |
C20 | 0.0474 (8) | 0.0823 (12) | 0.0654 (10) | −0.0013 (7) | 0.0004 (7) | 0.0195 (8) |
C21 | 0.0479 (8) | 0.0980 (13) | 0.0446 (7) | 0.0008 (8) | 0.0021 (6) | 0.0054 (8) |
C22 | 0.0492 (7) | 0.0756 (10) | 0.0393 (7) | 0.0082 (7) | −0.0030 (6) | −0.0022 (6) |
C23 | 0.0748 (10) | 0.0820 (11) | 0.0433 (7) | 0.0160 (9) | 0.0066 (7) | −0.0087 (7) |
C24 | 0.0911 (12) | 0.0642 (10) | 0.0543 (9) | 0.0173 (9) | 0.0047 (8) | −0.0130 (7) |
C25 | 0.0501 (7) | 0.0616 (8) | 0.0470 (7) | −0.0020 (6) | 0.0068 (6) | −0.0091 (6) |
C26 | 0.1010 (14) | 0.0730 (11) | 0.0481 (8) | 0.0112 (10) | 0.0018 (8) | 0.0013 (7) |
Geometric parameters (Å, º) top
N1—C8 | 1.368 (2) | C11—C14 | 1.5034 (18) |
N1—C1 | 1.363 (2) | C11—C12 | 1.524 (2) |
N1—H1 | 0.8600 | C11—H11 | 0.9800 |
N2—C10 | 1.458 (2) | C12—C16 | 1.506 (2) |
N2—C11 | 1.467 (2) | C12—C13 | 1.518 (2) |
N2—H2 | 0.8600 | C12—H12 | 0.9800 |
O1—C15 | 1.371 (2) | C13—H13A | 0.9700 |
O1—C16 | 1.435 (2) | C13—H13B | 0.9700 |
O2—C25 | 1.201 (2) | C14—C15 | 1.367 (2) |
O3—C25 | 1.325 (2) | C14—C17 | 1.430 (2) |
O3—C26 | 1.437 (2) | C15—C24 | 1.412 (2) |
C1—C2 | 1.399 (2) | C16—H16A | 0.9700 |
C1—C6 | 1.411 (2) | C16—H16B | 0.9700 |
C2—C3 | 1.369 (3) | C17—C18 | 1.412 (2) |
C2—H2A | 0.9300 | C17—C22 | 1.4214 (19) |
C3—C4 | 1.392 (3) | C18—C19 | 1.368 (2) |
C3—H3 | 0.9300 | C18—H18 | 0.9300 |
C4—C5 | 1.378 (3) | C19—C20 | 1.394 (2) |
C4—H4 | 0.9300 | C19—H19 | 0.9300 |
C5—C6 | 1.395 (2) | C20—C21 | 1.354 (3) |
C5—H5 | 0.9300 | C20—H20 | 0.9300 |
C6—C7 | 1.430 (2) | C21—C22 | 1.408 (2) |
C7—C8 | 1.359 (2) | C21—H21 | 0.9300 |
C7—C9 | 1.499 (2) | C22—C23 | 1.414 (2) |
C8—H8 | 0.9300 | C23—C24 | 1.350 (3) |
C9—C10 | 1.540 (2) | C23—H23 | 0.9300 |
C9—H9A | 0.9700 | C24—H24 | 0.9300 |
C9—H9B | 0.9700 | C26—H26A | 0.9600 |
C10—C25 | 1.518 (2) | C26—H26B | 0.9600 |
C10—C13 | 1.566 (2) | C26—H26C | 0.9600 |
| | | |
C8—N1—C1 | 108.79 (14) | C13—C12—H12 | 110.5 |
C8—N1—H1 | 125.6 | C11—C12—H12 | 110.5 |
C1—N1—H1 | 125.6 | C12—C13—C10 | 105.20 (11) |
C10—N2—C11 | 108.35 (10) | C12—C13—H13A | 110.7 |
C10—N2—H2 | 125.8 | C10—C13—H13A | 110.7 |
C11—N2—H2 | 125.8 | C12—C13—H13B | 110.7 |
C15—O1—C16 | 115.05 (12) | C10—C13—H13B | 110.7 |
C25—O3—C26 | 117.17 (13) | H13A—C13—H13B | 108.8 |
N1—C1—C2 | 130.75 (17) | C15—C14—C17 | 118.57 (13) |
N1—C1—C6 | 107.31 (15) | C15—C14—C11 | 120.14 (13) |
C2—C1—C6 | 121.94 (16) | C17—C14—C11 | 121.25 (12) |
C3—C2—C1 | 117.51 (19) | C14—C15—O1 | 123.45 (14) |
C3—C2—H2A | 121.2 | C14—C15—C24 | 121.67 (15) |
C1—C2—H2A | 121.2 | O1—C15—C24 | 114.89 (14) |
C2—C3—C4 | 121.51 (19) | O1—C16—C12 | 111.34 (13) |
C2—C3—H3 | 119.2 | O1—C16—H16A | 109.4 |
C4—C3—H3 | 119.2 | C12—C16—H16A | 109.4 |
C5—C4—C3 | 121.26 (19) | O1—C16—H16B | 109.4 |
C5—C4—H4 | 119.4 | C12—C16—H16B | 109.4 |
C3—C4—H4 | 119.4 | H16A—C16—H16B | 108.0 |
C4—C5—C6 | 119.05 (18) | C18—C17—C22 | 117.72 (14) |
C4—C5—H5 | 120.5 | C18—C17—C14 | 122.30 (13) |
C6—C5—H5 | 120.5 | C22—C17—C14 | 119.96 (13) |
C5—C6—C1 | 118.73 (16) | C19—C18—C17 | 121.13 (15) |
C5—C6—C7 | 133.94 (16) | C19—C18—H18 | 119.4 |
C1—C6—C7 | 107.33 (14) | C17—C18—H18 | 119.4 |
C8—C7—C6 | 105.77 (14) | C18—C19—C20 | 120.65 (16) |
C8—C7—C9 | 127.70 (15) | C18—C19—H19 | 119.7 |
C6—C7—C9 | 126.53 (13) | C20—C19—H19 | 119.7 |
C7—C8—N1 | 110.79 (15) | C21—C20—C19 | 119.83 (16) |
C7—C8—H8 | 124.6 | C21—C20—H20 | 120.1 |
N1—C8—H8 | 124.6 | C19—C20—H20 | 120.1 |
C7—C9—C10 | 114.22 (11) | C20—C21—C22 | 121.43 (15) |
C7—C9—H9A | 108.7 | C20—C21—H21 | 119.3 |
C10—C9—H9A | 108.7 | C22—C21—H21 | 119.3 |
C7—C9—H9B | 108.7 | C21—C22—C23 | 122.51 (14) |
C10—C9—H9B | 108.7 | C21—C22—C17 | 119.17 (15) |
H9A—C9—H9B | 107.6 | C23—C22—C17 | 118.31 (15) |
N2—C10—C25 | 109.73 (11) | C24—C23—C22 | 121.35 (15) |
N2—C10—C9 | 110.65 (12) | C24—C23—H23 | 119.3 |
C25—C10—C9 | 110.52 (11) | C22—C23—H23 | 119.3 |
N2—C10—C13 | 106.12 (11) | C23—C24—C15 | 120.10 (16) |
C25—C10—C13 | 108.66 (13) | C23—C24—H24 | 120.0 |
C9—C10—C13 | 111.05 (11) | C15—C24—H24 | 120.0 |
N2—C11—C14 | 112.74 (11) | O2—C25—O3 | 123.87 (14) |
N2—C11—C12 | 105.01 (11) | O2—C25—C10 | 125.47 (13) |
C14—C11—C12 | 113.47 (12) | O3—C25—C10 | 110.64 (12) |
N2—C11—H11 | 108.5 | O3—C26—H26A | 109.5 |
C14—C11—H11 | 108.5 | O3—C26—H26B | 109.5 |
C12—C11—H11 | 108.5 | H26A—C26—H26B | 109.5 |
C16—C12—C13 | 112.46 (13) | O3—C26—H26C | 109.5 |
C16—C12—C11 | 109.05 (12) | H26A—C26—H26C | 109.5 |
C13—C12—C11 | 103.69 (12) | H26B—C26—H26C | 109.5 |
C16—C12—H12 | 110.5 | | |
| | | |
C8—N1—C1—C2 | −179.51 (16) | C12—C11—C14—C15 | −7.98 (18) |
C8—N1—C1—C6 | 0.72 (18) | N2—C11—C14—C17 | −71.22 (16) |
N1—C1—C2—C3 | −179.27 (18) | C12—C11—C14—C17 | 169.57 (11) |
C6—C1—C2—C3 | 0.5 (2) | C17—C14—C15—O1 | 179.60 (13) |
C1—C2—C3—C4 | 0.0 (3) | C11—C14—C15—O1 | −2.8 (2) |
C2—C3—C4—C5 | −0.1 (3) | C17—C14—C15—C24 | −0.6 (2) |
C3—C4—C5—C6 | −0.3 (3) | C11—C14—C15—C24 | 177.00 (14) |
C4—C5—C6—C1 | 0.7 (2) | C16—O1—C15—C14 | −19.3 (2) |
C4—C5—C6—C7 | −179.53 (17) | C16—O1—C15—C24 | 160.92 (15) |
N1—C1—C6—C5 | 178.94 (14) | C15—O1—C16—C12 | 51.3 (2) |
C2—C1—C6—C5 | −0.9 (2) | C13—C12—C16—O1 | −174.29 (13) |
N1—C1—C6—C7 | −0.87 (16) | C11—C12—C16—O1 | −59.86 (18) |
C2—C1—C6—C7 | 179.35 (14) | C15—C14—C17—C18 | −176.39 (13) |
C5—C6—C7—C8 | −179.08 (17) | C11—C14—C17—C18 | 6.03 (19) |
C1—C6—C7—C8 | 0.68 (16) | C15—C14—C17—C22 | 2.03 (19) |
C5—C6—C7—C9 | 1.2 (3) | C11—C14—C17—C22 | −175.55 (11) |
C1—C6—C7—C9 | −179.09 (13) | C22—C17—C18—C19 | 1.7 (2) |
C6—C7—C8—N1 | −0.25 (18) | C14—C17—C18—C19 | −179.80 (13) |
C9—C7—C8—N1 | 179.52 (14) | C17—C18—C19—C20 | 0.6 (2) |
C1—N1—C8—C7 | −0.30 (19) | C18—C19—C20—C21 | −2.4 (2) |
C8—C7—C9—C10 | −76.46 (19) | C19—C20—C21—C22 | 1.7 (2) |
C6—C7—C9—C10 | 103.25 (16) | C20—C21—C22—C23 | −177.89 (15) |
C11—N2—C10—C25 | 133.38 (12) | C20—C21—C22—C17 | 0.7 (2) |
C11—N2—C10—C9 | −104.41 (13) | C18—C17—C22—C21 | −2.38 (19) |
C11—N2—C10—C13 | 16.15 (15) | C14—C17—C22—C21 | 179.13 (12) |
C7—C9—C10—N2 | −61.78 (16) | C18—C17—C22—C23 | 176.25 (13) |
C7—C9—C10—C25 | 59.97 (16) | C14—C17—C22—C23 | −2.24 (19) |
C7—C9—C10—C13 | −179.36 (12) | C21—C22—C23—C24 | 179.63 (15) |
C10—N2—C11—C14 | −155.72 (12) | C17—C22—C23—C24 | 1.0 (2) |
C10—N2—C11—C12 | −31.70 (15) | C22—C23—C24—C15 | 0.4 (3) |
N2—C11—C12—C16 | −85.90 (14) | C14—C15—C24—C23 | −0.6 (3) |
C14—C11—C12—C16 | 37.65 (15) | O1—C15—C24—C23 | 179.21 (15) |
N2—C11—C12—C13 | 34.10 (14) | C26—O3—C25—O2 | 1.6 (2) |
C14—C11—C12—C13 | 157.65 (12) | C26—O3—C25—C10 | 179.84 (14) |
C16—C12—C13—C10 | 93.76 (16) | N2—C10—C25—O2 | −12.0 (2) |
C11—C12—C13—C10 | −23.89 (15) | C9—C10—C25—O2 | −134.25 (16) |
N2—C10—C13—C12 | 5.55 (16) | C13—C10—C25—O2 | 103.66 (18) |
C25—C10—C13—C12 | −112.39 (13) | N2—C10—C25—O3 | 169.84 (12) |
C9—C10—C13—C12 | 125.85 (13) | C9—C10—C25—O3 | 47.56 (16) |
N2—C11—C14—C15 | 111.24 (15) | C13—C10—C25—O3 | −74.53 (15) |
Hydrogen-bond geometry (Å, º) top
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1···O2i | 0.86 | 2.38 | 3.075 (2) | 139 |
C26—H26C···O1ii | 0.96 | 2.42 | 3.209 (2) | 139 |
Symmetry codes: (i) −x+1, −y+1, −z+1; (ii) x, −y+1/2, z+1/2. |