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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20302생성일: 2026년 10월 24일

HCID 178452121, 화합물 → HCID 178452119, 화합물

https://huagongshe.com/ko/reaction/20302

반응식

참여 물질

역할이름HCID투입량
반응물HCID 178452121HCID 178452121—
촉매PalladiumHCID 23938—
용매N,N-dimethylformamide ethanolHCID 19794673—
생성물HCID 178452119HCID 17845211973.8%

반응 단계

4-[(4-Nitro-1H-pyrazole-3-carbonyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester (13.05 g) was dissolved in ethanol/DMF (300 ml/75 ml), treated with 10% palladium on carbon (500 mg) then hydrogenated at room temperature and pressure overnight. The catalyst was removed by filtration through Celite and the filtrate evaporated and re-evaporated with toluene. The crude material was purified by flash column chromatography eluting with EtOAc then 2% MeOH/EtOAc then 5% MeOH/EtOAc. Product containing fractions were combined and evaporated to give 8.78 g of 4-[(4-amino-1H-pyrazole-3-carbonyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester as a brown foam. (LC/MS: Rt 1.91, [M+H]+ 310).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745638B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6ce96a5154a4438bac2f558f0b1ed6a2
출처 메모uspto-grants-2010_06