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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375457Generated: October 29, 2026

Toluene → HCID 178441684, compound

https://huagongshe.com/reaction/375457

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 numberUS05484955
Source datasetuspto-grants-1996_01
ORD IDord-9dc48f35294e4532a2a7e2fb1e0a95a3
Source noteuspto-grants-1996_01