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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277485Generated: October 30, 2026

Azido(trimethyl)stannane → HCID 178467365, compound

https://huagongshe.com/reaction/277485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzido(trimethyl)stannaneHCID 5104973—
ReactantMethyl 1-[(2'-cyano[1,1'-biphenyl]-4-yl)methyl]-2-ethoxy-1H-benzimidazole-7-carboxylateHCID 15654674—
SolventTolueneHCID 1140—
ProductHCID 178467365HCID 17846736556.8%

Reaction Steps

A mixture of methyl 1-((2′-cyanobiphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-carboxylate (1.85 g) and trimethyltin azide (2.80 g) in toluene (15 ml) were heated under reflux for one day. The reaction mixture was concentrated to dryness. To the residue were added methanol (50 ml) and 1N-HCl (20 ml) and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was adjusted to about pH 3-4 with 1N-NaOH. After removal of the solvent, the residual syrup was purified by column chromatography on silica gel to give crystals. Recrystallization from ethyl acetate-benzene gave colorless crystals (1.16 g, 56%), m.p. 191-193° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355808B2
Source datasetuspto-grants-2002_03
ORD IDord-3aedb34a97654983a28aab0ee6a23176
Source noteuspto-grants-2002_03