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HRID 1450197作成日:2026年10月25日

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

https://huagongshe.com/reaction/1450197

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-MorpholinoethylamineHCID 408285—
反応物4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acidHCID 9863428—
反応物N,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chlorideHCID 19975454—
溶媒DichloromethaneHCID 6344—
生成物4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-N-(2-morpholin-4-yl-ethyl)-2phenyl-butyramideHCID 986916512.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602128
出典データセットuspto-grants-1997_02
ORD IDord-ca76bfaad1a34f2582baf40143769d3d
出典メモuspto-grants-1997_02