Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280574생성일: 2026년 10월 24일
Amlodipine → 4-(2-Chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-2-{2-[(2-chloro-5-pyridyl)sulphonamido]ethoxymethyl}-1,4-dihydropyridine
https://huagongshe.com/ko/reaction/280574
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Amlodipine | HCID 2162 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Chloro-5-pyridinesulfonyl chloride | HCID 2792792 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(2-Chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-2-{2-[(2-chloro-5-pyridyl)sulphonamido]ethoxymethyl}-1,4-dihydropyridine | HCID 23320840 | 54.8% |
반응 단계
A solution of 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine (409 mg) and triethylamine (202 mg) in dry dichloromethane (20 ml) was stirred under nitrogen and cooled in an ice-bath while a solution of 2-chloro-5-pyridinesulphonyl chloride (212 mg) in dry dichloromethane (10 ml) was added dropwise. The reaction mixture was allowed to warm to room temperature and stirring continued for a further 3 hours. The solvent was evaporated and the residue chromatographed on silica, eluting with dichloromethane. Appropriate fractions were combined and evaporated and the residue recrystallised from ethyl acetate to give the title compound (320 mg), m.p. 140°-140.5° C. Found: C, 51,27; H, 4.63; N, 7.25. C25H27Cl2N3O7 requires C, 51.37; H, 4.66; N, 7.19%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04590195 |
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| 출처 데이터셋 | uspto-grants-1986_05 |
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| ORD ID | ord-5c341f7cd88d44d39d32fefb43089a7a |
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| 출처 메모 | uspto-grants-1986_05 |
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