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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977403Generated: October 30, 2026

Azido(trimethyl)stannane → HCID 178456811, compound

https://huagongshe.com/reaction/1977403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzido(trimethyl)stannaneHCID 5104973—
ReactantHCID 15654687HCID 15654687—
SolventTolueneHCID 1140—
ProductHCID 178456811HCID 178456811758.9%

Reaction Steps

A solution of ethyl 1-[(2′-cyanobiphenyl-4-yl)methyl]-2-propylaminobenzimidazole-7-carboxylate (1.20 g) and trimethyltin azide (2.7 g) in toluene (15 ml) was heated for 50 hours under reflux. Precipitates were collected by filtration and suspended in methanol (20 ml). After addition of 1N-HCl (15 ml), the reaction mixture was stirred at room temperature for 10 minutes. The mixture was adjusted to about pH 5 with 1N-NaOH, followed by extraction with chloroform. The organic layer was washed with water, dried and concentrated to dryness. The concentrate was purified by column chromatography on silica gel to give crystals. Recrystallization from methanol-ethyl acetate gave colorless crystals (10 g, 77%), m.p. 170-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232334B1
Source datasetuspto-grants-2001_05
ORD IDord-f649c205b4e44da38b3b0bdeaff68581
Source noteuspto-grants-2001_05