참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| 반응물 | 4-(Aminomethyl)benzonitrile hydrochloride | HCID 9942250 | — |
| 생성물 | HCID 47298773 | HCID 47298773 | 89.5% |
반응 단계
Reaction was carried out in the same manner as in a Reference Example 2-(d) except for using 4-fluorobenzenesulfonyl chloride (1.18 g, 6.06 mmol) in place of 3-pyridylsulfonyl chloride, and using 4-cyanobenzylamine hydrochloride (1.00 g, 5.93 mmol) in place of (6-phenylpyridazin-3-ylmethyl)amine hydrochloride. After completion of the reaction, a saturated aqueous sodium chloride solution was added to the reaction solution, followed by extraction with ethyl acetate. The separated organic layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. To the resulting residue dissolved in a small amount of methylene chloride was added hexane, and a precipitated solid was collected by filtration. The resulting solid was dried under reduced pressure at 60° C. to afford the title compound (1.54 g) as a slightly brown solid. (Yield: 89%)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08648097B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-4f48ed52527942d3a31f8956d81718e2 |
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| 출처 메모 | uspto-grants-2014_02 |
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