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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256601생성일: 2026년 10월 25일

Isopropanol → Nilvadipine

https://huagongshe.com/reaction/256601

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Sodium CarbonateHCID 10340—
반응물Phosphorus pentachlorideHCID 24819—
반응물6-Cyano-5-methoxycarbonyl-2-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acidHCID 15388766—
용매DichloromethaneHCID 6344—
생성물NilvadipineHCID 449495.4%

반응 단계

In methylene chloride (30 ml) is suspended methyl (+)-5-carboxy-2-cyano-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate (3.12 g) followed by addition of phosphorus pentachloride (2.46 g) with ice-cooling, and the mixture is stirred for 30 minutes. Then, a solution of isopropyl alcohol (1.4 g) in methylene chloride (10 ml) is added dropwise over a period of 10 minutes. The mixture is stirred for 20 minutes, at the end of which time 5% aqueous sodium carbonate solution (30 ml) is added and the mixture is stirred at ambient temperature for one hour. The organic layer is separated and the water layer is extracted with methylene chloride. The organic layers are combined, washed with aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue is purified by silica gel (75 g) column chromatography, elution being carried out with benzeneethyl acetate (10:1). The solvent is removed from the eluate under reduced pressure and the residue is crystallized from diisopropyl ether to provide 5-isopropyl 3-methyl (+)-2-cyano-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate (3.34 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258393
출처 데이터셋uspto-grants-1993_11
ORD IDord-77bfd4d9bb8e4b79a65d1edd92bfbd1b
출처 메모uspto-grants-1993_11