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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357122Generated: November 3, 2026

Acetic Acid → (2RS,5SR)-3-[5-(4-Fluoro-phenyl)-1-(toluene-4-sulfonyl)-pyrrolidin-2-yl]-5-methyl-[1,2,4]oxadiazole

https://huagongshe.com/reaction/1357122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178427383HCID 178427383—
SolventDimethylformamideHCID 6228—
Product(2RS,5SR)-3-[5-(4-Fluoro-phenyl)-1-(toluene-4-sulfonyl)-pyrrolidin-2-yl]-5-methyl-[1,2,4]oxadiazoleHCID 2225047168%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of acetic acid (0.11 ml, 1.99 mmol), 1,1′-carbonyl-diimidazole (0.32 g, 1.99 mmol) in DMF (12 ml) was stirred at room temperature for 2 h and subsequently (2RS,5SR)-5-(4-fluoro-phenyl)-N-hydroxy-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxamidine (0.50 g, 1.32 mmol) was added. The reaction mixture was stirred at 80° C. for 16 h and evaporated. Acetic acid (10 ml) was added and the stirred mixture was heated under reflux conditions for 2 h. Aqueous work-up, column chromatography on silica gel (ethyl acetate/hexane 1:1) and crystallization from ethyl acetate/hexane yielded the title compound (0.36 g, yield 68%) as a white solid, m.p. 115° C. and MS: m/e=246.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589978B2
Source datasetuspto-grants-2003_07
ORD IDord-a02672f1cf8a45d595e34db2f998beef
Source noteuspto-grants-2003_07