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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242476생성일: 2026년 10월 25일

Isobutyl chloroformate → N-((S)-1-((S)-1-amino-4-methyl-1-oxopentan-2-ylamino)-3,3-dimethyl-1-oxobutan-2-yl)-5-methyl-3-(2,4,5-trifluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-carboxamide

https://huagongshe.com/reaction/242476

반응식

참여 물질

역할이름HCID투입량
반응물Isobutyl chloroformateHCID 62365—
반응물LeucinamideHCID 69640—
반응물DiisopropylethylamineHCID 81531—
반응물(S)-3,3-dimethyl-2-(5-methyl-3-(2,4,5-trifluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-carboxamido)butanoic acidHCID 46861922—
용매DichloromethaneHCID 6344—
생성물N-((S)-1-((S)-1-amino-4-methyl-1-oxopentan-2-ylamino)-3,3-dimethyl-1-oxobutan-2-yl)-5-methyl-3-(2,4,5-trifluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-carboxamideHCID 46861923—

반응 단계

To a solution of compound 71 (40 mg) in DCM was added DIEA (45 uL) followed by isobutylchloroformate (26 uL). After stirring at room temperature for 30 min, leucine amide (18 mg) and DIEA (25 uL) was added and stirred for 1 h. The reaction mixture was evaporated and dissolved in MeOH, and purified with a preparative LC-MS to give compound 72. LCMS (+ESI) m/z=537.3 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653127B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-eda2cff38ef04079b11b8b7e41454a5d
출처 메모uspto-grants-2014_02