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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1968424생성일: 2026년 10월 23일

[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitro-phenyl)-amine → N3-[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-4-methyl-benzene-1,3-diamine

https://huagongshe.com/ko/reaction/1968424

반응식

참여 물질

역할이름HCID투입량
반응물[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitro-phenyl)-amineHCID 15949047—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물N3-[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-4-methyl-benzene-1,3-diamineHCID 15948950—

반응 단계

[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitrophenyl)-amine (135 mg, 0.37 mmol) is dissolved in ethanol (30 mL). After hydrogenation catalyzed by palladium (10 wt % on activated carbon, wet, Degussa type, 22 mg) under 1 atm H2 balloon overnight, the reaction mixture is filtered through a pad of celite and washed with ethanol. The combined filtrate and washings are concentrated to afford the title compound, which is used for next reaction without any further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08426404B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-df738a17d522404a9b50ca0761e77f2b
출처 메모uspto-grants-2013_04