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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371823Generated: November 1, 2026

Diisopropylethylamine → (5R)-3-(3-Fluorophenyl)-5-[(4-methyl-1H-1,2,3-triazol-1-yl)methyl]-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/1371823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(5S)-5-(aminomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-oneHCID 11401559—
ReactantN'-[2,2-dichloro-1-methylethylidene]-4-methylbenzenesulfonohydrazideHCID 73181071—
SolventMethanolHCID 887—
Product(5R)-3-(3-Fluorophenyl)-5-[(4-methyl-1H-1,2,3-triazol-1-yl)methyl]-1,3-oxazolidin-2-oneHCID 5877831772%

Reaction Conditions

Temperature0 °C

Reaction Steps

N,N-Diisopropylethylamine (3.20 ml, 18.35 mmol) was added to a solution of (5S)-5-(aminomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-one (0.77 g, 3.57 mmol) (see Patent Application: Dong Pharmaceuticals WO 01/94342) in anhydrous methanol (25 ml). The solution was cooled to 0° C., and N′-[2,2-dichloro-1-methylethylidene]-4-methylbenzenesulfonohydrazide (1.28 g, 4.58 mmol) was added. The solution was warmed to room temperature and stirred overnight. The reaction mixture was then concentrated under vacuum and chromatographed on silica gel using 2% methanol/dichloromethane to give 0.71 g of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157482B2
Source datasetuspto-grants-2007_01
ORD IDord-a66e0f5d024a4afbb2a2cbffc7dac4a5
Source noteuspto-grants-2007_01