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HRID 637403作成日:2026年10月26日
Thiophene → 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine
https://huagongshe.com/reaction/637403
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thiophene | HCID 8030 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | Norastemizole hydrobromide | HCID 3018631 | — |
| 反応物 | 1-Benzyl-3-piperidone hydrochloride hydrate | HCID 3084924 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | 2-Methoxyethanol | HCID 8019 | — |
| 生成物 | 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine | HCID 13588070 | — |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04556660 |
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| 出典データセット | uspto-grants-1985_12 |
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| ORD ID | ord-8c3a50b0a37c4b588229f06d8f4bbcb9 |
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| 出典メモ | uspto-grants-1985_12 |
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