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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

反応式

関与物質

役割名称HCID仕込み量
反応物ThiopheneHCID 8030—
反応物Potassium AcetateHCID 517044—
反応物Norastemizole hydrobromideHCID 3018631—
反応物1-Benzyl-3-piperidone hydrochloride hydrateHCID 3084924—
反応物HCID 178418361HCID 178418361—
溶媒EthanolHCID 702—
溶媒2-MethoxyethanolHCID 8019—
生成物1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04556660
出典データセットuspto-grants-1985_12
ORD IDord-8c3a50b0a37c4b588229f06d8f4bbcb9
出典メモuspto-grants-1985_12