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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1496703생성일: 2026년 10월 27일

Water → (4R)-5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid

https://huagongshe.com/reaction/1496703

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanolHCID 5953—
반응물2,6-Dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid monomethyl esterHCID 173322—
용매MethanolHCID 887—
생성물(4R)-5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acidHCID 74847218.6%

반응 조건

온도90 °C

반응 단계

To a solution of 5-(methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid (700 g, 2.1 mol) in methanol (14 L) was added Quinidine (617 g, 1.90 mol). The mixture was stirred at 90° C. under reflux until Quinidine was completely dissolved. The stirring was continued for 3 hours. 4.5 L water was added. The stirring was continued for half an hour. The mixture was cooled down slowly. A solid was precipitated out and was filtered. The filter cake was treated with hydrochloric acid to produce (R)-5-(methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid (130 g) in a yield of 18.6%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09198902B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-f689c5b0769a49d5be4fb6ea37b8f1bb
출처 메모uspto-grants-2015_12