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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 711453생성일: 2026년 10월 26일

Methyl 6-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-cyano-2-(4-fluoro-3-methylphenylamino)nicotinate → tert-Butyl (1S,2R)-2-(4-(4-fluoro-3-methylphenylamino)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)cyclohexylcarbamate

https://huagongshe.com/reaction/711453

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참여 물질

역할이름HCID투입량
반응물Methyl 6-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-cyano-2-(4-fluoro-3-methylphenylamino)nicotinateHCID 67237937—
촉매Platinum oxide (PtO)HCID 82844—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
생성물tert-Butyl (1S,2R)-2-(4-(4-fluoro-3-methylphenylamino)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)cyclohexylcarbamateHCID 8665470770.6%

반응 단계

A mixture of methyl 6-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-cyano-2-(4-fluoro-3-methylphenylamino)nicotinate (75 mg, 0.151 mmol) and platinum oxide (34.2 mg, 0.151 mmol) in DCM (2 mL) and HOAc (0.5 mL) was stirred at RT under H2 atmosphere. The mixture was subsequently filtered through Celite. The filtrate was concentrated and the residue was purified by preparative HPLC to give the title compound (50 mg, 70.6%). [M+H] calc'd for C25H32FN5O3, 470. found, 470.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181255B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-8a024c68f77e492d88a8776f7203211b
출처 메모uspto-grants-2015_11