関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Mercaptoethanol | HCID 1567 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-2-chloroacetamide | HCID 19962925 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-2-(2-hydroxyethylthio)acetamide | HCID 19962907 | 77% |
反応手順
0.12 ml of 2-mercaptoethanol was added to a solution of 0.13 g of 85% potassium hydroxide and 0.50 g of N-[3-(4-piperidinomethyl-2-pyridyloxy)propyl]-2-chloroacetamide [prepared as described in step (a) above] in 10 ml methanol, and the resulting mixture was stirred at room temperature for 1 hour. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, the concentrate was mixed with water, and the resulting aqueous mixture was extracted with chloroform. The extract was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel, using a 1:9 by volume mixture of ethanol and chloroform as the eluent, to give 0.43 g (yield 77%) of the title compound as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05616579 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-19df28b2737b4a69a239e6d9146cc7db |
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| 出典メモ | uspto-grants-1997_04 |
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