Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369189Generated: October 28, 2026

Water → HCID 9847850, compound

https://huagongshe.com/reaction/369189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23285059HCID 23285059—
SolventDimethylformamideHCID 6228—
ProductHCID 9847850HCID 984785042.5%

Reaction Steps

120 mg of sodium hydride was added, under ice-cooling, to a solution of 1.0 g of 4-[N-methyl-N-(2-phenylethyl)amino]-1-[3-hydroxy-4-(1,2,4-triazol-1-yl)benzoyl]piperidine in 10 ml of dimethylformamide. The mixture was stirred for 1 hour. Thereto was dropwise added 320 mg of (2-chloroethyl)dimethylamine. The mixture was stirred at room temperature for 2 hours and then at 50° C. for 2 hours. The reaction mixture was poured into 50 ml of water. The mixture was extracted with three 50-ml portions of ethyl acetate. The extract was washed with 50 ml of a saturated aqueous sodium chloride solution, dried with magnesium sulfate, and subjected to distillation to remove the solvent. The residue was purified by a silica gel column chromatography (eluant: dichloromethane/methanol=10/1 to dichloromethane/methanol/ammonia water=100/10/1). The product was recrystallized from ethyl acetate-n-hexane to obtain 500 mg of 4-[N-methyl-N-(2-phenylethyl)amino]-1-[3-(2-dimethylaminoethoxy)-4-(1,2,4-triazol-1-yl)benzoyl]piperidine as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136826
Source datasetuspto-grants-2000_10
ORD IDord-b462f55a01664d02865e122b55bb4234
Source noteuspto-grants-2000_10