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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68857Generated: October 29, 2026

Ethyl Acetate → N-Cyclopropyl-N-[1-(5-methyl-pyrazin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide

https://huagongshe.com/reaction/68857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant2-Chloro-5-methylpyrazineHCID 12600386—
ReactantN-Cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamideHCID 68289931—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-Cyclopropyl-N-[1-(5-methyl-pyrazin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 68290609—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide (600 mg), 2-chloro-5-methyl-pyrazine (100 mg), and cesium carbonate (300 mg) in N,N-dimethylformamide (10 mL) is stirred for 3 days at 80° C. After cooling to room temperature ethyl acetate and water are added. The organic phase is separated, washed with water and brine, dried over MgSO4, and concentrated in vacuo. The residue is chromatographed on silica gel (ethyl acetate/methanol 7:3) to give the title compound. LC (method 1): tR=1.08 min; Mass spectrum (ESI+): m/z=404 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822471B2
Source datasetuspto-grants-2014_09
ORD IDord-8b26fe2d26d141b59329e926cf0a860e
Source noteuspto-grants-2014_09