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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370621Generated: October 28, 2026

Bromomethyl acetate → HCID 69942568, compound

https://huagongshe.com/reaction/1370621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl acetateHCID 68536—
ReactantHCID 3002971HCID 3002971—
SolventAcetonitrileHCID 6342—
ProductHCID 69942568HCID 69942568—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 1-[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]-3-[4-(1H-1,2,3-triazol-1-yl)phenyl]-2-imidazolidinone (0.5 g) and acetonitrile (10 ml) was added bromomethyl acetate (0.1 ml), and the mixture was stirred for 24 hours at 50° C. The reaction mixture was purified by silica gel flush chromatography (silica gel 25 g, eluent: ethyl acetate→acetone→acetone/ethanol=10/1). The residue purified was crystallized from ethanol to give 4-acetoxymethyl-1-[(2R,3R)-2-(2,4-difluorophenyl)-2-hydroxy-3-[2-oxo-3-[4-(1H-1,2,3-triazol-1-yl)phenyl]-1-imidazolidinyl]butyl]-1H-1,2,4-triazolium bromide (Compound 10, 0.135 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583164B1
Source datasetuspto-grants-2003_06
ORD IDord-17e6feea34914d519e5ca3a168c8441a
Source noteuspto-grants-2003_06