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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2248145생성일: 2026년 10월 26일

(+)-1,4-Dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid benzyl ester → (+)-1,4-Dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/2248145

반응식

참여 물질

역할이름HCID투입량
반응물(+)-1,4-Dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid benzyl esterHCID 13923228—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물(+)-1,4-Dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acidHCID 13670941—

반응 단계

1.6 g (0.00331 mole) (+)-1,4-dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid benzyl ester is taken up in 32 mL ethanol and hydrogenated without the use of pressure at 20° C. in the presence of 0.64 g 10% palladium/charcoal (50% moist). The catalyst is filtered off and the filtrate evaporated to dryness at 35° C. on a rotary evaporator. The solid residue is recrystallized from 10 mL diisopropyl ether. The product is dried at 40° C. in a vacuum drying cabinet; yield: 1.04 g (80.3% of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05037987
출처 데이터셋uspto-grants-1991_08
ORD IDord-343b204245df41179317667a1a247851
출처 메모uspto-grants-1991_08