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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845781생성일: 2026년 10월 25일

Ammonia → N-[1-(2-aminopropyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/845781

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물1-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]-2-propanoneHCID 13588076—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
용매MethanolHCID 887—
생성물N-[1-(2-aminopropyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amineHCID 1358807834%

반응 단계

A mixture of 4 parts of 1-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]-2-propanone, oxime and 120 parts of methanol, saturated with ammonia, was hydrogenated at normal pressure and at room temperature with 2 parts of Raney-nickel catalyst. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was crystallized from acetonitrile, yielding 1.3 parts (34%) of N-[1-(2-aminopropyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amine, mp. 178.3° C. (intermediate 132).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04760074
출처 데이터셋uspto-grants-1988_07
ORD IDord-866bd65f0a434de795c034088ebd20e9
출처 메모uspto-grants-1988_07