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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392964Generated: October 28, 2026

Azido(trimethyl)stannane → HCID 178420385, compound

https://huagongshe.com/reaction/392964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzido(trimethyl)stannaneHCID 5104973—
Reactant2-[4-(Benzyloxy)phenyl]-1-cyclohexyl-1H-benzimidazole-5-carbonitrileHCID 22660790—
SolventTolueneHCID 1140—
ProductHCID 178420385HCID 17842038520%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803374B2
Source datasetuspto-grants-2004_10
ORD IDord-57347641a7f24669b1426a447d0b47fa
Source noteuspto-grants-2004_10