참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Pyridinemethanamine | HCID 19509 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 4-(3-Hydroxypropylthio)pyridine | HCID 19079134 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(3-(N-2-pyridylmethylamino)propylthio]pyridine | HCID 19079176 | 25.4% |
반응 단계
To a solution of 5.26 g (31.1 mmol) of 4-(3-hydroxypropylthio)pyridine and 5.20 ml (37.3 mmol) of triethylamine in 150 ml of methylene chloride, 2.90 ml (37.3 mmol) of methanesulfonyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried, and then the solvent was distilled off. To 6.33 g of the residue was added 2.64 ml (25.6 mmol) of 2-aminomethylpyridine. The resulting mixture was heated at 80° C. for 3 hours. After cooling, the mixture was purified by column chromatography (eluent: chloroform/methanol=25:1) to obtain 1.62 g of the desired compound (yield: 25.4%, yellow oil).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05246948 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-9a9a1fc08b224050b6bc9bda7fc64182 |
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| 출처 메모 | uspto-grants-1993_09 |
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