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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856250Generated: October 25, 2026

Dimethylformamide → 2-Methyl-6-nitro-2-[4-(4-trifluoromethylbenzoyl)piperidin-1-yl]methyl-2,3-dihydroimidazo[2,1-b]oxazole

https://huagongshe.com/reaction/856250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium AcetateHCID 517045—
Reactant4-(4-Trifluoromethylbenzoyl)piperidineHCID 11637455—
Reactant2-Chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazoleHCID 15965523—
SolventWaterHCID 962—
Product2-Methyl-6-nitro-2-[4-(4-trifluoromethylbenzoyl)piperidin-1-yl]methyl-2,3-dihydroimidazo[2,1-b]oxazoleHCID 6948309329%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazole prepared in Example 6 (80 mg, 0.37 mmol), 4-(4-trifluoromethylbenzoyl)piperidine (95 mg, 0.37 mmol), sodium acetate (150 mg, 1.83 mmol) and DMF (2 ml) was stirred at 80° C. overnight. The reaction mixture was poured into water, and extracted with ethyl acetate twice. The organic phases were combined, washed with water three times, washed with a saturated saline solution, dried over sodium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=1/1) to afford 2-methyl-6-nitro-2-[4-(4-trifluoromethylbenzoyl)piperidin-1-yl]methyl-2,3-dihydroimidazo[2,1-b]oxazole (46 mg, yield 29%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-20cf7a1eeea74674948a0059cc2514ee
Source noteuspto-grants-2007_08