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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18472생성일: 2026년 10월 25일

Water → HCID 66997065, 화합물

https://huagongshe.com/reaction/18472

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물p-Toluenesulfonic acidHCID 6101—
반응물(S)-3'-(3,4-difluorophenyl)-N-(3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-6',7'-dihydrospiro[[1,3]dioxolane-2,5'-indazole]-1'(4'H)-carboxamideHCID 46863561—
반응물3-(3,4-difluorophenyl)-N-((S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-5-hydroxy-4,5,6,7-tetrahydro-1H-indazole-1-carboxamideHCID 46863563—
용매AcetoneHCID 180—
생성물HCID 66997065HCID 6699706591%

반응 단계

Preparation of 3-(3,4-difluorophenyl)-N—((S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-5-hydroxy-4,5,6,7-tetrahydro-1H-indazole-1-carboxamide (67) A mixture of compound 63 (0.91 g) and p-toluenesulfonic acid (1.3 g) was heated in acetone and water at 50° C. until starting material was consumed. After evaporation of acetone, the residue was extracted between EtOAc and saturated sodium bicarbonate. The organic phase was dried over sodium sulfate and evaporated to dryness. The crude product was purified by column chromatography with 70% to 80% EtOAc/Hex to give (S)-3-(3,4-difluorophenyl)-N-(3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-5-oxo-4,5,6,7-tetrahydro-1H-indazole-1-carboxamide (0.75 g, 91% yield), which was reduced with sodium borohydride (1.0 equiv.) in MeOH to give compound 67 as a mixture of two diastereomers after purification with a preparative LC-MS. LCMS (+ESI) m/z=421.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741350B1
출처 데이터셋uspto-grants-2010_06
ORD IDord-728e1c0d78d54310a6b3e1121a47319a
출처 메모uspto-grants-2010_06