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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

반응식

참여 물질

역할이름HCID투입량
반응물AmlodipineHCID 2162—
반응물TriethylamineHCID 8471—
반응물2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
용매DichloromethaneHCID 6344—
생성물4-(2-Chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-2-{2-[(2-chloro-5-pyridyl)sulphonamido]ethoxymethyl}-1,4-dihydropyridineHCID 2332084054.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04590195
출처 데이터셋uspto-grants-1986_05
ORD IDord-5c341f7cd88d44d39d32fefb43089a7a
출처 메모uspto-grants-1986_05