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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246704생성일: 2026년 10월 24일

1,3-Cyclohexanediamine → N-(3-aminocyclohexyl)-2-bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide

https://huagongshe.com/ko/reaction/246704

반응식

참여 물질

역할이름HCID투입량
반응물1,3-CyclohexanediamineHCID 18814—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 86677897—
용매DimethylformamideHCID 6228—
생성물N-(3-aminocyclohexyl)-2-bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxamideHCID 86678005—

반응 단계

A mixture of 2-bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (0.2 g, 0.83 mmol), cyclohexane-1,3-diamine (0.473 g, 4.15 mmol), HATU (0.475 g, 1.25 mmol), DIPEA (0.322 g, 2.5 mmol) in 15 mL of DMF were stirred at room temperature overnight. The solvent was removed under reduced pressure at 70° C. to give N-(3-aminocyclohexyl)-2-bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide as a crude which was used to the next step without further purification. MS: (M+H)+=338.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658646B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-399e91d6b945443188c43a9458f89d22
출처 메모uspto-grants-2014_02