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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986263생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/986263

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물(+)-1,4-Dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid benzyl esterHCID 13923228—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물(+)-1,4-Dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acidHCID 13670941—

반응 단계

Three g (6.2 mMol) Benzyl (±)-1,4-dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylate are hydrogenated at normal pressure and at ambient temperature with the use of 1.5 g. 10% palladium on active charcoal in 100 ml. ethanol. The take up of hydrogen is finished after 30 minutes. The catalyst is filtered off, the solvent is distilled off in a vacuum and the colorless, crystalline residue is recrystallized from diisopropyl ether/ethyl acetate. There is obtained (±)-1,4-dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid in the form of colorless crystals with a melting point of 164°-166° C. (decomp.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04711901
출처 데이터셋uspto-grants-1987_12
ORD IDord-2feab84a74fa4d99a6333450f608ff2c
출처 메모uspto-grants-1987_12