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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637403생성일: 2026년 10월 25일

Thiophene → 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/637403

반응식

참여 물질

역할이름HCID투입량
반응물ThiopheneHCID 8030—
반응물Potassium AcetateHCID 517044—
반응물Norastemizole hydrobromideHCID 3018631—
반응물1-Benzyl-3-piperidone hydrochloride hydrateHCID 3084924—
반응물HCID 178418361HCID 178418361—
용매EthanolHCID 702—
용매2-MethoxyethanolHCID 8019—
생성물1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amineHCID 13588070—

반응 단계

A mixture of 25 parts of 1-(phenylmethyl)-3-piperidinone hydrochloride, 55 parts of 1-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-1H-benzimidazol-2-amine dihydrobromide, 1 parts of a solution of thiophene in ethanol 4%, 50 parts of potassium acetate and 500 parts of 2-methoxyethanol was hydrogenated at normal pressure and at 50° C. with 5 parts of palldium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in water and the whole was alkalized with sodium hydroxide. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized twice from acetonitrile. The product was filtered off and dried, yielding 9.75 parts of 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine; mp. 174.6° C. (intermediate 70).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04556660
출처 데이터셋uspto-grants-1985_12
ORD IDord-8c3a50b0a37c4b588229f06d8f4bbcb9
출처 메모uspto-grants-1985_12