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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410288Generated: November 1, 2026

Dichloromethane → HCID 886827, compound

https://huagongshe.com/reaction/2410288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-(Piperidin-1-yl)-5-(trifluoromethyl)anilineHCID 694756—
SolventWaterHCID 962—
ProductHCID 886827HCID 88682786.7%

Reaction Steps

Benzoyl chloride (50.0 μl, 0.430 mmol, commercially available product) and triethylamine (170 μl, 1.21 mmol) were sequentially added at 0° C. to a dichloromethane (3 ml) solution of 2-(1-piperidinyl)-5-(trifluoromethyl)aniline (102 mg, 0.417 mmol), obtained as described in Referential Example 1-2. The resulting mixture was warmed to room temperature and stirred for 18 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=10/1). Thus, N-[2-(1-piperidinyl)-5-(trifluoromethyl)phenyl]benzamide (GIF-0344) (126 mg, 86.7%) was yielded as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816089B2
Source datasetuspto-grants-2014_08
ORD IDord-f1a1e956b16b44a6873e2ac3e3081cd0
Source noteuspto-grants-2014_08