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HRID 1904824作成日:2026年10月25日
1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine → 1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine
https://huagongshe.com/reaction/1904824
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine | HCID 14518094 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine | HCID 20037906 | 58.5% |
反応手順
A mixture of 16 parts of 1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine and 160 parts of methanol was hydrogenated at normal pressure and at 50° C. with 5 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. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97.5:2.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The oily residue was crystallized from 14 parts of 1,1'-oxybisethane. The product was filtered off and dried, yielding 7.8 parts (58.5%) of 1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridine; mp. 159.3° C. (32).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04839374 |
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| 出典データセット | uspto-grants-1989_06 |
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| ORD ID | ord-b76ae46e401845598f01e357c0f225b2 |
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| 出典メモ | uspto-grants-1989_06 |
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