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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497899Generated: October 29, 2026

1,1'-Carbonyldiimidazole → 5-(2-Fluorocyclopropyl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1497899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactantrac-(1R,2S)-2-fluorocyclopropane-1-carboxylic acidHCID 10103129—
ReactantN'-hydroxy-4-methyl-3-nitrobenzimidamideHCID 73711052—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-(2-Fluorocyclopropyl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazoleHCID 71280729—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirring solution of trans-2-Fluoro-cyclopropanecarboxylic acid (0.38 g, 3.68 mmol) in anhydrous NMP (12 mL) was added 1,1′-carbonyldiimidazole (CDI) (0.59 g, 3.68 mmol). The reaction was stirred for 3 minutes. N′-hydroxy-4-methyl-3-nitrobenzimidamide (27) (0.72 g, 3.68 mmol) was added and the reaction was stirred for minutes then heated in the microwave at 120° C. for 15 minutes. The crude product was extracted with ethyl acetate. The organic layer was washed with water, brine and dried over anhydrous sodium sulfate. The solvent was concentrated and the crude product was purified on silica gel using ethyl acetate and hexane to yield 5-(2-fluorocyclopropyl)-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole (129). MS m/z 264.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199981B2
Source datasetuspto-grants-2015_12
ORD IDord-b01aa1f4299d4e5c921b463be0f6a826
Source noteuspto-grants-2015_12