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HRID 893676생성일: 2026년 10월 24일

Ammonia → N6-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]-amino]-1-piperidinyl]ethyl]-2,3,6-pyridinetriamine

https://huagongshe.com/ko/reaction/893676

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물ThiopheneHCID 8030—
반응물N6-[2-[4-[[1-[(4-fluorophenyl)methyl]1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]-3-nitro-2,6-pyridinediamineHCID 13588113—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물N6-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]-amino]-1-piperidinyl]ethyl]-2,3,6-pyridinetriamineHCID 1498986794%

반응 단계

A mixture of 10 parts of N6 -[2-[4-[[1-[(4fluorophenyl)methyl]-1H-benzimidazol-2yl]amino]-1-piperidinyl]ethyl]-3-nitro-2,6-pyridinediamine, 3 parts of a solution of thiophene in methanol 4% and 400 parts of methanol, saturated with ammonia, was hydrogenated at normal pressure and at room temperature with 4 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated, yielding 9 parts (94%) of N6 -[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]-2,3,6-pyridinetriamine as a residue (intermediate 154).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05126339
출처 데이터셋uspto-grants-1992_06
ORD IDord-48e0fc932fe640c8a84c1b4f237ac936
출처 메모uspto-grants-1992_06