Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466456Generated: October 31, 2026

Azido(trimethyl)stannane → 1-[(2'-(Trimethylstannyltetrazol-5-yl)biphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazole

https://huagongshe.com/reaction/466456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzido(trimethyl)stannaneHCID 5104973—
Reactant4'-((2-Butyl-4-chloro-5-(hydroxymethyl)-1H-imidazol-1-yl)methyl)(1,1'-biphenyl)-2-carbonitrileHCID 14425664—
Product1-[(2'-(Trimethylstannyltetrazol-5-yl)biphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazoleHCID 14425665—

Reaction Conditions

Temperature115 °C

Reaction Steps

1-[(2'-Cyanobiphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazole (766 g), trimethyl tin azide (766 g) and xylenes (7.90 L) were charged to a 12 liter round-bottomed flask equipped with mechanical stirrer, condenser with N2 inlet and thermometer contained in a heating mantle. The slurry was heated to 115° C., giving a clear solution, and held for 41 hours. The resulting slurry was cooled to room temperature and the crude product isolated by vacuum filtration, washed with toluene (800 ml) and dried in vacuo at ~50° C. overnight. The crude product (1202 g) was charged to a 12 liter round-bottomed flask and slurried at 105° C. with toluene (70 L). The slurry was cooled to 50° C. and the product isolated by vacuum filtration, washed with one liter of toluene and dried in vacuo at 50° C. overnight. Yield: 1071 g, 94%. M.P.: 211°-214° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155118
Source datasetuspto-grants-1992_10
ORD IDord-f670f1d90ec348fa8061d696f0508b79
Source noteuspto-grants-1992_10