Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807059478/bt2620sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807059478/bt2620Isup2.hkl |
CCDC reference: 672981
Key indicators
- Single-crystal X-ray study
- T = 200 K
- Mean (C-C) = 0.003 Å
- R factor = 0.052
- wR factor = 0.126
- Data-to-parameter ratio = 21.4
checkCIF/PLATON results
No syntax errors found
Alert level C PLAT242_ALERT_2_C Check Low Ueq as Compared to Neighbors for Si1 PLAT242_ALERT_2_C Check Low Ueq as Compared to Neighbors for Si2
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 2 ALERT type 2 Indicator that the structure model may be wrong or deficient 0 ALERT type 3 Indicator that the structure quality may be low 0 ALERT type 4 Improvement, methodology, query or suggestion 0 ALERT type 5 Informative message, check
The title compound was prepared according to a published procedure for the bis(trimethylsilyl) derivative (Franchetti et al., 2004).
The title compound was prepared in analogy to a published procedure (Franchetti et al., 2004) upon reaction of nicotineamide with chlorotrimethylsilane in boiling hexamethyldisilazane. Crystals suitable for X-ray analysis were obtained within one day after slowly cooling down the reaction mixture.
All H atoms were located in a difference map and refined as riding on their parent atoms with Caromatic—H = 0.95 Å, Cmethyl—H = 0.98 Å and N—H = 0.88 Å. Two common isotropic displacement parameters for the H atoms were refined: one for the methyl Hs and one for the remaining Hs.
Data collection: COLLECT (Nonius, 2000); cell refinement: HKL SCALEPACK (Otwinowski & Minor, 1997); data reduction: HKL DENZO and SCALEPACK (Otwinowski & Minor, 1997); program(s) used to solve structure: SIR97 (Altomare et al., 1999); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ORTEPIII (Burnett & Johnson, 1996); software used to prepare material for publication: SHELXL97 (Sheldrick, 1997).
C9H14N2OSi | Z = 4 |
Mr = 194.31 | F(000) = 416 |
Triclinic, P1 | Dx = 1.149 Mg m−3 |
Hall symbol: -P 1 | Mo Kα radiation, λ = 0.71073 Å |
a = 9.9550 (3) Å | Cell parameters from 3640 reflections |
b = 11.0928 (4) Å | θ = 3.1–27.5° |
c = 11.2096 (4) Å | µ = 0.18 mm−1 |
α = 80.5113 (14)° | T = 200 K |
β = 82.6627 (13)° | Needle, colourless |
γ = 67.2202 (19)° | 0.18 × 0.06 × 0.03 mm |
V = 1122.91 (7) Å3 |
KappaCCD diffractometer | 3244 reflections with I > 2σ(I) |
Radiation source: rotating anode | Rint = 0.030 |
MONTEL, graded multilayered X-ray optics monochromator | θmax = 27.5°, θmin = 3.3° |
ϕ/ω–scan | h = −12→12 |
7682 measured reflections | k = −14→12 |
5073 independent reflections | l = −13→14 |
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)] = 0.052 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.126 | Only H-atom displacement parameters refined |
S = 1.01 | w = 1/[σ2(Fo2) + (0.0385P)2 + 0.342P] where P = (Fo2 + 2Fc2)/3 |
5073 reflections | (Δ/σ)max < 0.001 |
237 parameters | Δρmax = 0.20 e Å−3 |
0 restraints | Δρmin = −0.24 e Å−3 |
C9H14N2OSi | γ = 67.2202 (19)° |
Mr = 194.31 | V = 1122.91 (7) Å3 |
Triclinic, P1 | Z = 4 |
a = 9.9550 (3) Å | Mo Kα radiation |
b = 11.0928 (4) Å | µ = 0.18 mm−1 |
c = 11.2096 (4) Å | T = 200 K |
α = 80.5113 (14)° | 0.18 × 0.06 × 0.03 mm |
β = 82.6627 (13)° |
KappaCCD diffractometer | 3244 reflections with I > 2σ(I) |
7682 measured reflections | Rint = 0.030 |
5073 independent reflections |
R[F2 > 2σ(F2)] = 0.052 | 0 restraints |
wR(F2) = 0.126 | Only H-atom displacement parameters refined |
S = 1.01 | Δρmax = 0.20 e Å−3 |
5073 reflections | Δρmin = −0.24 e Å−3 |
237 parameters |
x | y | z | Uiso*/Ueq | ||
Si1 | 0.70081 (7) | 0.07672 (6) | 0.13501 (6) | 0.04635 (18) | |
Si2 | 0.15496 (6) | 0.20555 (7) | 0.41313 (6) | 0.04568 (18) | |
O1 | 0.42748 (15) | 0.31010 (16) | 0.16768 (15) | 0.0530 (4) | |
O2 | −0.05206 (15) | 0.23814 (16) | 0.23110 (14) | 0.0519 (4) | |
N1 | 0.6058 (2) | 0.5495 (2) | 0.3814 (2) | 0.0594 (6) | |
N2 | 0.66665 (17) | 0.22227 (17) | 0.19744 (16) | 0.0436 (4) | |
H721 | 0.7404 | 0.2323 | 0.2246 | 0.056 (2)* | |
N3 | −0.0520 (3) | 0.3866 (2) | −0.1337 (2) | 0.0665 (6) | |
N4 | 0.15327 (17) | 0.26542 (17) | 0.25745 (15) | 0.0384 (4) | |
H741 | 0.2223 | 0.2940 | 0.2244 | 0.056 (2)* | |
C1 | 0.6209 (2) | 0.4456 (2) | 0.3272 (2) | 0.0500 (6) | |
H1 | 0.7110 | 0.3723 | 0.3325 | 0.056 (2)* | |
C2 | 0.5146 (2) | 0.4372 (2) | 0.26416 (19) | 0.0392 (5) | |
C3 | 0.3823 (2) | 0.5446 (2) | 0.2575 (2) | 0.0504 (6) | |
H3 | 0.3052 | 0.5434 | 0.2163 | 0.056 (2)* | |
C4 | 0.3658 (3) | 0.6531 (2) | 0.3123 (2) | 0.0560 (6) | |
H4 | 0.2775 | 0.7285 | 0.3080 | 0.056 (2)* | |
C5 | 0.4783 (3) | 0.6506 (2) | 0.3727 (2) | 0.0555 (6) | |
H5 | 0.4645 | 0.7254 | 0.4106 | 0.056 (2)* | |
C6 | 0.5334 (2) | 0.3194 (2) | 0.20598 (19) | 0.0411 (5) | |
C7 | 0.8928 (3) | −0.0263 (3) | 0.1667 (3) | 0.0643 (7) | |
H71 | 0.9013 | −0.0455 | 0.2545 | 0.116 (3)* | |
H72 | 0.9561 | 0.0212 | 0.1304 | 0.116 (3)* | |
H73 | 0.9226 | −0.1090 | 0.1319 | 0.116 (3)* | |
C8 | 0.6801 (3) | 0.1152 (3) | −0.0291 (3) | 0.0777 (9) | |
H81 | 0.5780 | 0.1699 | −0.0437 | 0.116 (3)* | |
H82 | 0.7087 | 0.0331 | −0.0648 | 0.116 (3)* | |
H83 | 0.7427 | 0.1630 | −0.0663 | 0.116 (3)* | |
C9 | 0.5745 (3) | −0.0029 (3) | 0.2113 (3) | 0.0724 (8) | |
H91 | 0.5881 | −0.0228 | 0.2984 | 0.116 (3)* | |
H92 | 0.5949 | −0.0848 | 0.1775 | 0.116 (3)* | |
H93 | 0.4735 | 0.0568 | 0.1983 | 0.116 (3)* | |
C10 | −0.0537 (2) | 0.3488 (2) | −0.0142 (2) | 0.0526 (6) | |
H10 | −0.1427 | 0.3475 | 0.0270 | 0.056 (2)* | |
C11 | 0.0669 (2) | 0.3113 (2) | 0.05355 (18) | 0.0383 (5) | |
C12 | 0.1957 (2) | 0.3146 (2) | −0.0080 (2) | 0.0466 (5) | |
H12 | 0.2807 | 0.2914 | 0.0345 | 0.056 (2)* | |
C13 | 0.1991 (3) | 0.3517 (3) | −0.1311 (2) | 0.0589 (6) | |
H13 | 0.2869 | 0.3524 | −0.1752 | 0.056 (2)* | |
C14 | 0.0738 (3) | 0.3878 (2) | −0.1894 (2) | 0.0640 (7) | |
H14 | 0.0770 | 0.4152 | −0.2742 | 0.056 (2)* | |
C15 | 0.0515 (2) | 0.2697 (2) | 0.18614 (19) | 0.0381 (5) | |
C16 | 0.1900 (3) | 0.0272 (3) | 0.4290 (3) | 0.0713 (8) | |
H161 | 0.2827 | −0.0184 | 0.3845 | 0.116 (3)* | |
H162 | 0.1106 | 0.0146 | 0.3958 | 0.116 (3)* | |
H163 | 0.1951 | −0.0088 | 0.5149 | 0.116 (3)* | |
C17 | 0.3083 (3) | 0.2331 (3) | 0.4661 (2) | 0.0678 (7) | |
H171 | 0.2875 | 0.3279 | 0.4570 | 0.116 (3)* | |
H172 | 0.3984 | 0.1893 | 0.4177 | 0.116 (3)* | |
H173 | 0.3201 | 0.1967 | 0.5516 | 0.116 (3)* | |
C18 | −0.0187 (3) | 0.2966 (3) | 0.4963 (2) | 0.0765 (9) | |
H181 | −0.0342 | 0.3904 | 0.4864 | 0.116 (3)* | |
H182 | −0.0141 | 0.2620 | 0.5826 | 0.116 (3)* | |
H183 | −0.0997 | 0.2857 | 0.4640 | 0.116 (3)* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Si1 | 0.0443 (3) | 0.0472 (4) | 0.0531 (4) | −0.0208 (3) | −0.0041 (3) | −0.0118 (3) |
Si2 | 0.0445 (3) | 0.0535 (4) | 0.0421 (4) | −0.0217 (3) | −0.0064 (3) | −0.0035 (3) |
O1 | 0.0354 (8) | 0.0616 (11) | 0.0699 (11) | −0.0227 (7) | −0.0111 (7) | −0.0124 (8) |
O2 | 0.0333 (8) | 0.0691 (11) | 0.0613 (10) | −0.0260 (7) | −0.0024 (7) | −0.0133 (8) |
N1 | 0.0482 (11) | 0.0602 (14) | 0.0773 (15) | −0.0230 (10) | 0.0032 (10) | −0.0287 (11) |
N2 | 0.0330 (9) | 0.0456 (11) | 0.0584 (12) | −0.0181 (8) | −0.0070 (8) | −0.0120 (9) |
N3 | 0.0791 (16) | 0.0530 (14) | 0.0612 (15) | −0.0072 (11) | −0.0350 (12) | −0.0109 (11) |
N4 | 0.0328 (8) | 0.0492 (11) | 0.0400 (10) | −0.0219 (8) | −0.0061 (7) | −0.0049 (8) |
C1 | 0.0351 (11) | 0.0513 (14) | 0.0667 (15) | −0.0160 (10) | −0.0003 (10) | −0.0190 (12) |
C2 | 0.0328 (10) | 0.0418 (12) | 0.0448 (12) | −0.0179 (9) | 0.0018 (8) | −0.0038 (9) |
C3 | 0.0406 (12) | 0.0540 (15) | 0.0517 (14) | −0.0135 (10) | −0.0066 (10) | −0.0013 (11) |
C4 | 0.0543 (14) | 0.0454 (14) | 0.0564 (15) | −0.0077 (11) | 0.0042 (12) | −0.0081 (12) |
C5 | 0.0574 (15) | 0.0522 (15) | 0.0613 (16) | −0.0245 (12) | 0.0078 (12) | −0.0181 (12) |
C6 | 0.0320 (10) | 0.0475 (13) | 0.0475 (13) | −0.0200 (9) | −0.0024 (9) | −0.0031 (10) |
C7 | 0.0514 (14) | 0.0542 (16) | 0.0832 (19) | −0.0107 (12) | −0.0054 (13) | −0.0195 (14) |
C8 | 0.082 (2) | 0.095 (2) | 0.0586 (17) | −0.0306 (17) | −0.0094 (14) | −0.0191 (16) |
C9 | 0.0713 (17) | 0.0576 (17) | 0.098 (2) | −0.0358 (14) | 0.0067 (15) | −0.0151 (15) |
C10 | 0.0473 (13) | 0.0516 (14) | 0.0590 (16) | −0.0110 (11) | −0.0187 (11) | −0.0148 (12) |
C11 | 0.0364 (10) | 0.0363 (12) | 0.0435 (12) | −0.0101 (9) | −0.0096 (9) | −0.0122 (9) |
C12 | 0.0468 (12) | 0.0511 (14) | 0.0445 (13) | −0.0184 (10) | −0.0063 (10) | −0.0104 (11) |
C13 | 0.0734 (17) | 0.0567 (16) | 0.0459 (14) | −0.0233 (13) | 0.0030 (12) | −0.0121 (12) |
C14 | 0.097 (2) | 0.0452 (15) | 0.0425 (14) | −0.0141 (14) | −0.0152 (14) | −0.0091 (11) |
C15 | 0.0285 (10) | 0.0399 (12) | 0.0480 (12) | −0.0114 (8) | −0.0065 (8) | −0.0120 (9) |
C16 | 0.0840 (19) | 0.0589 (18) | 0.0745 (19) | −0.0346 (15) | −0.0060 (15) | 0.0026 (14) |
C17 | 0.0763 (18) | 0.088 (2) | 0.0530 (15) | −0.0437 (16) | −0.0251 (13) | 0.0016 (14) |
C18 | 0.0653 (17) | 0.101 (2) | 0.0498 (16) | −0.0157 (16) | 0.0027 (13) | −0.0176 (16) |
Si1—N2 | 1.7604 (18) | C7—H71 | 0.9800 |
Si1—C8 | 1.838 (3) | C7—H72 | 0.9800 |
Si1—C9 | 1.852 (3) | C7—H73 | 0.9800 |
Si1—C7 | 1.853 (2) | C8—H81 | 0.9800 |
Si2—N4 | 1.7617 (18) | C8—H82 | 0.9800 |
Si2—C18 | 1.851 (3) | C8—H83 | 0.9800 |
Si2—C17 | 1.852 (2) | C9—H91 | 0.9800 |
Si2—C16 | 1.852 (3) | C9—H92 | 0.9800 |
O1—C6 | 1.234 (2) | C9—H93 | 0.9800 |
O2—C15 | 1.237 (2) | C10—C11 | 1.390 (3) |
N1—C5 | 1.331 (3) | C10—H10 | 0.9500 |
N1—C1 | 1.339 (3) | C11—C12 | 1.387 (3) |
N2—C6 | 1.351 (3) | C11—C15 | 1.489 (3) |
N2—H721 | 0.8800 | C12—C13 | 1.374 (3) |
N3—C14 | 1.330 (4) | C12—H12 | 0.9500 |
N3—C10 | 1.336 (3) | C13—C14 | 1.370 (4) |
N4—C15 | 1.350 (2) | C13—H13 | 0.9500 |
N4—H741 | 0.8800 | C14—H14 | 0.9500 |
C1—C2 | 1.384 (3) | C16—H161 | 0.9800 |
C1—H1 | 0.9500 | C16—H162 | 0.9800 |
C2—C3 | 1.392 (3) | C16—H163 | 0.9800 |
C2—C6 | 1.493 (3) | C17—H171 | 0.9800 |
C3—C4 | 1.385 (3) | C17—H172 | 0.9800 |
C3—H3 | 0.9500 | C17—H173 | 0.9800 |
C4—C5 | 1.369 (3) | C18—H181 | 0.9800 |
C4—H4 | 0.9500 | C18—H182 | 0.9800 |
C5—H5 | 0.9500 | C18—H183 | 0.9800 |
N2—Si1—C8 | 109.72 (12) | H81—C8—H82 | 109.5 |
N2—Si1—C9 | 109.61 (11) | Si1—C8—H83 | 109.5 |
C8—Si1—C9 | 111.13 (14) | H81—C8—H83 | 109.5 |
N2—Si1—C7 | 103.89 (10) | H82—C8—H83 | 109.5 |
C8—Si1—C7 | 110.88 (13) | Si1—C9—H91 | 109.5 |
C9—Si1—C7 | 111.36 (14) | Si1—C9—H92 | 109.5 |
N4—Si2—C18 | 111.29 (11) | H91—C9—H92 | 109.5 |
N4—Si2—C17 | 104.79 (10) | Si1—C9—H93 | 109.5 |
C18—Si2—C17 | 110.26 (14) | H91—C9—H93 | 109.5 |
N4—Si2—C16 | 108.14 (11) | H92—C9—H93 | 109.5 |
C18—Si2—C16 | 111.33 (14) | N3—C10—C11 | 124.0 (2) |
C17—Si2—C16 | 110.82 (13) | N3—C10—H10 | 118.0 |
C5—N1—C1 | 116.3 (2) | C11—C10—H10 | 118.0 |
C6—N2—Si1 | 123.55 (14) | C12—C11—C10 | 117.2 (2) |
C6—N2—H721 | 118.2 | C12—C11—C15 | 123.86 (18) |
Si1—N2—H721 | 118.2 | C10—C11—C15 | 119.0 (2) |
C14—N3—C10 | 116.9 (2) | C13—C12—C11 | 119.2 (2) |
C15—N4—Si2 | 123.40 (14) | C13—C12—H12 | 120.4 |
C15—N4—H741 | 118.3 | C11—C12—H12 | 120.4 |
Si2—N4—H741 | 118.3 | C14—C13—C12 | 119.0 (2) |
N1—C1—C2 | 124.7 (2) | C14—C13—H13 | 120.5 |
N1—C1—H1 | 117.6 | C12—C13—H13 | 120.5 |
C2—C1—H1 | 117.6 | N3—C14—C13 | 123.6 (2) |
C1—C2—C3 | 117.4 (2) | N3—C14—H14 | 118.2 |
C1—C2—C6 | 123.68 (19) | C13—C14—H14 | 118.2 |
C3—C2—C6 | 118.94 (19) | O2—C15—N4 | 119.9 (2) |
C4—C3—C2 | 118.4 (2) | O2—C15—C11 | 120.82 (17) |
C4—C3—H3 | 120.8 | N4—C15—C11 | 119.24 (17) |
C2—C3—H3 | 120.8 | Si2—C16—H161 | 109.5 |
C5—C4—C3 | 119.2 (2) | Si2—C16—H162 | 109.5 |
C5—C4—H4 | 120.4 | H161—C16—H162 | 109.5 |
C3—C4—H4 | 120.4 | Si2—C16—H163 | 109.5 |
N1—C5—C4 | 123.9 (2) | H161—C16—H163 | 109.5 |
N1—C5—H5 | 118.0 | H162—C16—H163 | 109.5 |
C4—C5—H5 | 118.0 | Si2—C17—H171 | 109.5 |
O1—C6—N2 | 120.3 (2) | Si2—C17—H172 | 109.5 |
O1—C6—C2 | 120.15 (18) | H171—C17—H172 | 109.5 |
N2—C6—C2 | 119.52 (17) | Si2—C17—H173 | 109.5 |
Si1—C7—H71 | 109.5 | H171—C17—H173 | 109.5 |
Si1—C7—H72 | 109.5 | H172—C17—H173 | 109.5 |
H71—C7—H72 | 109.5 | Si2—C18—H181 | 109.5 |
Si1—C7—H73 | 109.5 | Si2—C18—H182 | 109.5 |
H71—C7—H73 | 109.5 | H181—C18—H182 | 109.5 |
H72—C7—H73 | 109.5 | Si2—C18—H183 | 109.5 |
Si1—C8—H81 | 109.5 | H181—C18—H183 | 109.5 |
Si1—C8—H82 | 109.5 | H182—C18—H183 | 109.5 |
C8—Si1—N2—C6 | 68.8 (2) | C3—C2—C6—O1 | −10.0 (3) |
C9—Si1—N2—C6 | −53.5 (2) | C1—C2—C6—N2 | −10.2 (3) |
C7—Si1—N2—C6 | −172.58 (18) | C3—C2—C6—N2 | 171.14 (19) |
C18—Si2—N4—C15 | −57.1 (2) | C14—N3—C10—C11 | −0.1 (4) |
C17—Si2—N4—C15 | −176.31 (17) | N3—C10—C11—C12 | 0.4 (3) |
C16—Si2—N4—C15 | 65.44 (19) | N3—C10—C11—C15 | −179.3 (2) |
C5—N1—C1—C2 | 0.1 (4) | C10—C11—C12—C13 | −1.1 (3) |
N1—C1—C2—C3 | −0.5 (4) | C15—C11—C12—C13 | 178.5 (2) |
N1—C1—C2—C6 | −179.2 (2) | C11—C12—C13—C14 | 1.6 (3) |
C1—C2—C3—C4 | 0.9 (3) | C10—N3—C14—C13 | 0.6 (4) |
C6—C2—C3—C4 | 179.7 (2) | C12—C13—C14—N3 | −1.4 (4) |
C2—C3—C4—C5 | −1.1 (3) | Si2—N4—C15—O2 | 4.5 (3) |
C1—N1—C5—C4 | −0.3 (4) | Si2—N4—C15—C11 | −174.82 (14) |
C3—C4—C5—N1 | 0.9 (4) | C12—C11—C15—O2 | −162.3 (2) |
Si1—N2—C6—O1 | −0.9 (3) | C10—C11—C15—O2 | 17.3 (3) |
Si1—N2—C6—C2 | 177.98 (15) | C12—C11—C15—N4 | 17.0 (3) |
C1—C2—C6—O1 | 168.7 (2) | C10—C11—C15—N4 | −163.37 (19) |
D—H···A | D—H | H···A | D···A | D—H···A |
N2—H721···O2i | 0.88 | 2.10 | 2.948 (2) | 161 |
N4—H741···O1 | 0.88 | 2.13 | 2.982 (2) | 164 |
C12—H12···O1 | 0.95 | 2.30 | 3.201 (3) | 157 |
C1—H1···O2i | 0.95 | 2.49 | 3.343 (3) | 149 |
C3—H3···N3ii | 0.95 | 2.58 | 3.492 (4) | 161 |
Symmetry codes: (i) x+1, y, z; (ii) −x, −y+1, −z. |
Experimental details
Crystal data | |
Chemical formula | C9H14N2OSi |
Mr | 194.31 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 200 |
a, b, c (Å) | 9.9550 (3), 11.0928 (4), 11.2096 (4) |
α, β, γ (°) | 80.5113 (14), 82.6627 (13), 67.2202 (19) |
V (Å3) | 1122.91 (7) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.18 |
Crystal size (mm) | 0.18 × 0.06 × 0.03 |
Data collection | |
Diffractometer | KappaCCD diffractometer |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 7682, 5073, 3244 |
Rint | 0.030 |
(sin θ/λ)max (Å−1) | 0.649 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.052, 0.126, 1.01 |
No. of reflections | 5073 |
No. of parameters | 237 |
H-atom treatment | Only H-atom displacement parameters refined |
Δρmax, Δρmin (e Å−3) | 0.20, −0.24 |
Computer programs: COLLECT (Nonius, 2000), HKL SCALEPACK (Otwinowski & Minor, 1997), HKL DENZO and SCALEPACK (Otwinowski & Minor, 1997), SIR97 (Altomare et al., 1999), SHELXL97 (Sheldrick, 1997), ORTEPIII (Burnett & Johnson, 1996).
D—H···A | D—H | H···A | D···A | D—H···A |
N2—H721···O2i | 0.88 | 2.10 | 2.948 (2) | 161 |
N4—H741···O1 | 0.88 | 2.13 | 2.982 (2) | 164 |
C12—H12···O1 | 0.95 | 2.30 | 3.201 (3) | 157 |
C1—H1···O2i | 0.95 | 2.49 | 3.343 (3) | 149 |
C3—H3···N3ii | 0.95 | 2.58 | 3.492 (4) | 161 |
Symmetry codes: (i) x+1, y, z; (ii) −x, −y+1, −z. |
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The title compound, silylated nicotineamide, is a building block for the synthesis of coenzymes of the NAD family. In contrast to the results presented by Franchetti et al. (2004), numerous variations of the reaction conditions always yielded the mono- instead of the bis-silyl derivative of nicotineamide. In order to verify Si-NMR-spectroscopic hints on monosilylation, the product was crystallized and structurally characterized.
In the crystal structure, two molecules with a different orientation of the pyridine-N atoms with respect to the amide function are stacked at right angles. The strongest intermolecular interactions are N–H···O hydrogen bonds (Fig. 1), the O acceptor thus being the stronger one compared with the potential pyridine-N acceptor. The latter acts as an acceptor in a weak C–H···N interaction, which, together with supporting π-stacking, connects two N–H···O-connected chains along [100] to double chains (Fig. 2).