Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195649Generated: October 26, 2026

Dichloromethane → 4-methoxy-N-[2-piperidin-1-yl-5-(trifluoromethyl)phenyl]benzamide

https://huagongshe.com/reaction/2195649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant2-(Piperidin-1-yl)-5-(trifluoromethyl)anilineHCID 694756—
SolventWaterHCID 962—
Product4-methoxy-N-[2-piperidin-1-yl-5-(trifluoromethyl)phenyl]benzamideHCID 1422797—

Reaction Steps

4-Methoxybenzoyl chloride (250 mg, 1.47 mmol, commercially available product) and triethylamine (254 μl, 1.83 mmol) were sequentially added at 0° C. to a dichloromethane (4 ml) solution of 2-(1-piperidinyl)-5-(trifluoromethyl)aniline (147 mg, 0.602 mmol), obtained as described in Referential Example 1-2. The resulting mixture was warmed to room temperature and stirred for 17 hours. Water was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20 g, hexane/ethyl acetate=5/1). Thus, N-[2-(1-piperidinyl)-5-(trifluoromethyl)phenyl]-4-methoxybenzamide (GIF-0615) (240 mg, quant.) was yielded as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338362B2
Source datasetuspto-grants-2012_12
ORD IDord-cc346b2d4d44467794281ecf43a31928
Source noteuspto-grants-2012_12