Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974935Generated: November 1, 2026

Triethylamine → HCID 19099543, compound

https://huagongshe.com/reaction/1974935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 19099540HCID 19099540—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19099543HCID 19099543—

Reaction Steps

A stirred solution of 0.250 g of 2-butyl-6-(hydroxymethyl)-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-4(3H)-quinazolinone and 0.246 ml of triethylamine in 5.0 ml of tetrahydrofuran is cooled to -78° C. and 0.137 ml of methanesulfonyl chloride added. The reaction mixture is allowed to warm to room temperature and continue stirring for 18 hours. The reaction mixture is partitioned between chloroform and water. The organic layer is washed with aqueous 5% HCl, water and saturated aqueous sodium bicarbonate then dried with magnesium suflate and evaporated to afford 0.278 g of the desired product. FAB MASS SPEC 787 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05284852
Source datasetuspto-grants-1994_02
ORD IDord-4e0b0f491bb642619c24833515107ea3
Source noteuspto-grants-1994_02