HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392964Generated: October 28, 2026
Azido(trimethyl)stannane → HCID 178420385, compound
https://huagongshe.com/reaction/392964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | 2-[4-(Benzyloxy)phenyl]-1-cyclohexyl-1H-benzimidazole-5-carbonitrile | HCID 22660790 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178420385 | HCID 178420385 | 20% |
Reaction Steps
A suspension of compound 12 (0.041 g, 0.10 mmol) and trimethyltin azide (0.023 g, 0.11 mmol) in toluene (2 mL) was refluxed for 15 h. The reaction mixture was allowed to stand at rt for 48 h. The resulting suspension was filtered and washed with toluene (2×). The solid was treated with hydrogen chloride (4 M in dioxane, several mL) for 4 h at rt. The reaction mixture was concentrated on a rotary evaporator. The residue was purified by reverse phase HPLC (C18 column, water/acetonitrile gradient containing 0.05% trifluoroacetic acid) to afford 13 as a white solid (0.009 g, 20%). 1H NMR (CDCl3) δ 8.22 (br s, 1H), 8.05 (br m, 1H), 7.82 (br m, 3H), 7.52-7.38 (m, 5H), 7.30 (br m, 2H), 5.23 (s, 2H), 4.53 (br m, 1H), 2.27 (br m, 4H), 2.06 (br m, 2H), 1.84 (br m, 1H), 1.40 (br m, 3H); ESI-MS m/e 451.3 (M+1); HPLC purity (ELSD)>95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06803374B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-57347641a7f24669b1426a447d0b47fa |
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| Source note | uspto-grants-2004_10 |
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