関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Morpholinoethylamine | HCID 408285 | — |
| 反応物 | 4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acid | HCID 9863428 | — |
| 反応物 | N,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chloride | HCID 19975454 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-N-(2-morpholin-4-yl-ethyl)-2phenyl-butyramide | HCID 9869165 | 12.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05602128 |
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| 出典データセット | uspto-grants-1997_02 |
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| ORD ID | ord-ca76bfaad1a34f2582baf40143769d3d |
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| 出典メモ | uspto-grants-1997_02 |
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