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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

反応式

関与物質

役割名称HCID仕込み量
反応物1-benzoyl-1,4-dihydro-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridineHCID 14518094—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物1-benzoyl-4-[(1-methyl-1H-benzimidazol-2-yl)methyl]pyridineHCID 2003790658.5%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04839374
出典データセットuspto-grants-1989_06
ORD IDord-b76ae46e401845598f01e357c0f225b2
出典メモuspto-grants-1989_06