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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424539Generated: November 1, 2026

Water → N-Cyclopropyl-4-oxazol-5-yl-N-[1-(3,3,3-trifluoro-propyl)-piperidin-4-yl]-benzamide

https://huagongshe.com/reaction/1424539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1,1-Trifluoro-3-iodopropaneHCID 156165—
ReactantN-Cyclopropyl-N-[1-(2-hydroxy-2-methyl-propyl)-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 86709612—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-Cyclopropyl-4-oxazol-5-yl-N-[1-(3,3,3-trifluoro-propyl)-piperidin-4-yl]-benzamideHCID 73053285—

Reaction Steps

A mixture of N-cyclopropyl-N-[1-(2-hydroxy-2-methyl-propyl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide (80 mg), 1-iodo-3,3,3-trifluoropropane (108 mg), and K2CO3 (63 mg) in N-methyl-2-pyrrolidone (2 mL) is stirred at room temperature for 4 h and then at 60° C. over night. Since conversion of starting material is still incomplete, K2CO3 (63 mg) and two portions of 1-iodo-3,3,3-trifluoropropane (54 mg each) are added while stirring the reaction mixture for two more days at 80° C. Water is added to the reaction mixture and the aqueous phase is extracted with ethyl acetate. The combined extracts are washed with brine dried over MgSO4 and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 75:25→50:50). The crude product is triturated with diethyl ether, filtered off, and dried to give the title compound. LC (method 3): tR=1.08 min; Mass spectrum (ESI+): m/z=408 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927726B2
Source datasetuspto-grants-2015_01
ORD IDord-72727667cb7944d2b81d083c7f7ccb4e
Source noteuspto-grants-2015_01