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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450197Generated: October 25, 2026

Triethylamine → 4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-N-(2-morpholin-4-yl-ethyl)-2phenyl-butyramide

https://huagongshe.com/reaction/1450197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-MorpholinoethylamineHCID 408285—
Reactant4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acidHCID 9863428—
ReactantN,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chlorideHCID 19975454—
SolventDichloromethaneHCID 6344—
Product4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-N-(2-morpholin-4-yl-ethyl)-2phenyl-butyramideHCID 986916512.9%

Reaction Steps

A mixture of 4-[4-(2-methoxyphenyl)piperazin-l-yl]-2-phenylbutanoic acid (3.544 g, 10 mmole), triethylamine (2.024 g, 20 mmole), and N,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chloride (2.545 g. 10 mmole) was stirred in methylene chloride (80 mL) under exclusion of moisture at ambient temperature for 30 minutes, after which 4-(2-aminoethyl)morpholine (1.302 g, 10 mmole) was added. The reaction mixture was stirred at room temperature for 14 hours, washed with water (100 ml), dried over magnesium sulfate, filtered and evaporated to dryness in vacuo. Chromatography on silica gel with methanol/chloroform as eluant, followed by crystallization from ethanol/diethyl ether with addition of ethanolic HCl gave 0.6 g of the title compound as the dihydrochloride, 2.5 hydrate, 0.2 CHCl3 solvate, m.p. 60°-5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602128
Source datasetuspto-grants-1997_02
ORD IDord-ca76bfaad1a34f2582baf40143769d3d
Source noteuspto-grants-1997_02