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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186913Generated: October 29, 2026

Acetonitrile → HCID 69944025, compound

https://huagongshe.com/reaction/2186913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantHCID 3002971HCID 3002971—
ReactantChloromethyl isopropyl carbonateHCID 14787051—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 69944025HCID 6994402527.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

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), chloromethyl isopropyl carbonate (3.2 g) and acetonitrile (1 ml) was stirred for 25 hours at 100° C. After having been cooled, the mixture was diluted with diisopropyl ether (10 ml), and the resulting powder was collected by filtration and subjected to the silica gel column chromatography (eluent: ethyl acetate→acetone→acetone/ethanol=10/1→acetone/ethanol=5/1). Solvent was distilled off under reduced pressure, and residue was subjected to crystallization from ethyl acetate. The crystals were dissolved in water (10 ml). The aqueous solution was lyophilized to give 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]-4-[(isopropoxycarbonyloxy)methyl]-1H-1,2,4-triazolium chloride (Compound 9, 0.18 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407129B1
Source datasetuspto-grants-2002_06
ORD IDord-e9da61e087234e57834e1bc79c6eb7d7
Source noteuspto-grants-2002_06