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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130489생성일: 2026년 10월 25일

Acetic Acid → 2-[6-(4-Iodo-phenyl)-7-oxo-3-trifluoromethyl-4,5,6,7-tetrahydro-pyrazolo[3,4-c]pyridin-1-yl]-5-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/130489

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물HydrazineHCID 9321—
반응물5-Methoxyanthranilic acidHCID 277930—
반응물3-hydroxy-1-(4-iodophenyl)-4-(2,2,2-trifluoroacetyl)-5,6-dihydro-1H-pyridin-2-oneHCID 21936834—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물2-[6-(4-Iodo-phenyl)-7-oxo-3-trifluoromethyl-4,5,6,7-tetrahydro-pyrazolo[3,4-c]pyridin-1-yl]-5-methoxy-benzoic acid methyl esterHCID 6930990324%

반응 조건

온도0 °C

반응 단계

Part A: To a 0° C. solution of 5-methoxyanthranilic acid (5.0 g, 29.9 mmol) in concentrated hydrochloric acid (10 mL) was added dropwise an ice cold solution of sodium nitrite (2.06 g, 29.9 mmol) in water (5 mL) and stirring was continued at 0° C. for 30 minutes. Stannous chloride dihydrate (16.8 g, 74.8 mmol) was dissolved in concentrated hydrochloric acid (16 mL), cooled to 0° C., and added slowly to the solution of the diazonium salt. The precipitate was agitated, kept at 0° C. for 30 minutes, and then filtered. The solids were washed successively with ice cold brine and petroleum ether and dried under a stream of air and then under vacuum. The crude hydrazine salt and 3-hydroxy-1-(4-iodo-phenyl)-4-(2,2,2-trifluoro-acetyl)-5,6-dihydro-1H-pyridin-2-one (12.3 g, 29.9 mmol) were combined in glacial acetic acid (50 mL) and heated to 80° C. Upon completion of the reaction the solvent was evaporated to a viscous oil which was subjected to silica gel column chromatography to yield 2-[6-(4-iodo-phenyl)-7-oxo-3-trifluoromethyl-4,5,6,7-tetrahydro-pyrazolo[3,4-c]pyridin-1-yl]-5-methoxy-benzoic acid methyl ester (4.12 g, 24%). MS (AP+) 571.9 (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381732B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-11c57d060ab843ceaed0c56790e5a790
출처 메모uspto-grants-2008_06