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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070506Generated: November 2, 2026

Triethylamine → N-[1-(3,4-dichlorobenzyl)-4-piperidinyl]-2-(3-phenyl-1H-1,2,4-triazol-5-yl)acetamide

https://huagongshe.com/reaction/1070506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant(3-Phenyl-1H-1,2,4-triazol-5-yl)acetic acidHCID 17609309—
Reactant1-(3,4-Dichloro-benzyl)-piperidin-4-ylamine hydrochlorideHCID 22396206—
SolventDichloromethaneHCID 6344—
ProductN-[1-(3,4-dichlorobenzyl)-4-piperidinyl]-2-(3-phenyl-1H-1,2,4-triazol-5-yl)acetamideHCID 2239617570.9%

Reaction Steps

(3-Phenyl-1H-1,2,4-triazol-5-yl)acetic acid (0.020 g) and N,N′-carbonyl diimidazole (0.016 g) in dichloromethane was stirred under nitrogen for 3 minutes. 1-(3,4-Dichlorobenzyl)-4-piperidinamine hydrochloride (0.031 g) and triethylamine (0.036 g) was then added and allowed to stir for 1 hour under nitrogen. Saturated sodium hydrogen carbonate was added to the reaction with the resulting solution being extracted three times with dichloromethane. The pooled organic phases were washed once with water, once with brine, dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to a white solid. This was purified by RPHPLC (75%-5%, 0.1% ammonium acetate/acetonitrile). Saturated sodium hydrogen carbonate was added to the pooled collected fractions with the resulting solution being extracted three times with dichloromethane. The pooled organic phases were washed once with water, once with brine, dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to leave N-[1-(3,4-dichlorobenzyl)-4-piperidinyl]-2-(3-phenyl-1H-1,2,4-triazol-5-yl)acetamide(0.031 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903085B1
Source datasetuspto-grants-2005_06
ORD IDord-8a5c7eb50fd24581ae810e34f692c325
Source noteuspto-grants-2005_06