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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Thiophene | HCID 8030 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | Norastemizole hydrobromide | HCID 3018631 | — |
| 반응물 | 1-Benzyl-3-piperidone hydrochloride hydrate | HCID 3084924 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | 2-Methoxyethanol | HCID 8019 | — |
| 생성물 | 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04556660 |
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| 출처 데이터셋 | uspto-grants-1985_12 |
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| ORD ID | ord-8c3a50b0a37c4b588229f06d8f4bbcb9 |
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| 출처 메모 | uspto-grants-1985_12 |
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