Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186909Generated: October 30, 2026

Acetonitrile → HCID 178461838, compound

https://huagongshe.com/reaction/2186909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantChloromethyl pivalateHCID 87885—
Reactant181869-54-5HCID 3002973—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 178461838HCID 17846183848.8%

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-tetrazol-1-yl)phenyl]-2-imidazolidinone(0.5 g), chloromethyl pivalate (15.7 g) and acetonitrile (2.4 g) was stirred for 6.5 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. The powder was subjected to silica gel column chromatography (eluent: ethyl acetate→acetone→acetone/ethanol=10/1→acetone/ethanol=5/1) to give 1-[(2R,3R)-2-(2,4-difluorophenyl)-2-hydroxy-3-[2-oxo-3-[4-(1H-tetrazol-1-yl)phenyl]-1-imidazolidinyl]butyl]-4-[(2,2-dimethylpropanoyloxy)methyl]-1H-1,2,4-triazolium chloride(Compound 2, 0.32 g) as a white powder. The above Compound 2 (0.4 g) was crystallized from ethyl acetate (20 ml) to give white crystals (0.3 g) of Compound 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407129B1
Source datasetuspto-grants-2002_06
ORD IDord-f377ecc0160546b09dbadf72834c1cf0
Source noteuspto-grants-2002_06