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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1450197생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1450197

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-MorpholinoethylamineHCID 408285—
반응물4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acidHCID 9863428—
반응물N,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chlorideHCID 19975454—
용매DichloromethaneHCID 6344—
생성물4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-N-(2-morpholin-4-yl-ethyl)-2phenyl-butyramideHCID 986916512.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05602128
출처 데이터셋uspto-grants-1997_02
ORD IDord-ca76bfaad1a34f2582baf40143769d3d
출처 메모uspto-grants-1997_02