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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449698Generated: October 30, 2026

Toluene → HCID 178441684, compound

https://huagongshe.com/reaction/1449698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4'-((2-Butyl-4-chloro-5-(hydroxymethyl)-1H-imidazol-1-yl)methyl)(1,1'-biphenyl)-2-carbonitrileHCID 14425664—
ReactantAzido(trioctyl)stannaneHCID 71354122—
SolventDimethylformamideHCID 6228—
ProductHCID 178441684HCID 17844168494.7%

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of 5 g of 2-butyl-4-chloro-1-[(2'-cyanobiphenyl-4-yl)methyl]-5-(hydroxymethyl)imidazole, 30.2 g of trioctyltin azide (tri-n-octyltin azide), 25 ml of toluene and 1 ml of dimethylformamide was stirred for 24 hours at 115° C. in nitrogen streams. The reaction mixture was, after cooling, concentrated, and there were added 40 ml of ethanol and a solution of 5.2 g of sodium nitrite in 19 ml of water, whose pH was adjusted at 3.4 with conc. hydrochloric acid. The resultant mixture was subjected to extraction with methylene chloride, and the extract was concentrated under reduced pressure. To the concentrate was added hexane, then resulting crystalline precipitates were collected by filtration. The crystals were washed with hexane, then dried to afford 5.27 g (yield 94.7%) of 2-butyl-4-chloro-5-(hydroxymethyl)-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]imidazole. The NMR spectrum of the product was in good agreement with that described in J. Med. Chem., 1991, 34, 2525.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599943
Source datasetuspto-grants-1997_02
ORD IDord-b474b3b3e81e458cb696d831223d1cb6
Source noteuspto-grants-1997_02