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HRID 964006作成日:2026年10月26日

4-Carbamoyl-1-(3-methoxyphenyl)pyridinium chloride → 1-(3-Methoxyphenyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/964006

反応式

関与物質

役割名称HCID仕込み量
反応物4-Carbamoyl-1-(3-methoxyphenyl)pyridinium chlorideHCID 10611695—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物1-(3-Methoxyphenyl)piperidine-4-carboxamideHCID 1060974782.6%

反応手順

A suspension of 4-carbamoyl-1-(3-methoxyphenyl)-pyridinium chloride (26 g) in methanol (300 ml) was hydrogenated at ambient temperature and pressure in the presence of 10% palladium-on-carbon catalyst (2.0 g) until hydrogen uptake ceased (~2 days) The mixture was filtered, excess triethylamine added and the solvent removed in vacuo to give a pink solid. This was partitioned between water and chloroform. The organic phase was dried and the solvent removed in vacuo to give 1-(3-methoxyphenyl)piperidine-4-carboxamide as a pink solid (19 g), m.p. 153°-156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05767116
出典データセットuspto-grants-1998_06
ORD IDord-77d34deed1904da48785faccfa985f19
出典メモuspto-grants-1998_06