Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5744생성일: 2026년 10월 23일
4-Hydroxybenzaldehyde → N-{2-[4-Chloro-N-(4-hydroxybenzyl) cinnamylamino]ethyl}-5-isoquinolinesulfonamide
https://huagongshe.com/ko/reaction/5744
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Hydroxybenzaldehyde | HCID 126 | — |
| 반응물 | N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide | HCID 176156 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-{2-[4-Chloro-N-(4-hydroxybenzyl) cinnamylamino]ethyl}-5-isoquinolinesulfonamide | HCID 53642189 | 59.3% |
반응 단계
0.2 g of the product of Example 172 and 0.13 g of p-hydroxybenzaldehyde were dissolved in 10 ml of methanol, to the solution were added 60 mg of sodium cyanoborohydride and two drops of acetic acid, and the mixture was stirred for 2 days at a room temperature. The reaction mixture was concentrated under a reduced pressure, and after adding a saturated sodium chloride aqueous solution, extracted three times with 20 ml of ethyl acetate. The extracts were combined, washed with sodium chloride, dried over magnesium sulfate, filtered and concentrated under a reduced pressure. The resulting residue was purified on a silica gel column (silica gel 10 g, eluant: 2% methanol in chloroform), to obtain 150 mg of the title compound in a colorless amorphous form.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05245034 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-ad93cea3c46c4c05874b445fc5c954fd |
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| 출처 메모 | uspto-grants-1993_09 |
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