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HRID 25970作成日:2026年10月24日

1-Benzyl-4-piperidone → N~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamine

https://huagongshe.com/ja/reaction/25970

反応式

関与物質

役割名称HCID仕込み量
反応物1-Benzyl-4-piperidoneHCID 19220—
反応物1,2-Ethanediamine, N1-phenyl-HCID 74270—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
生成物N~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamineHCID 20540168—

反応手順

To the solution of 12.6 g of N-phenylethylenediamine in 200 ml of methanol, 50 ml of 4.1 N ethanolic hydrogen chloride are added dropwise followed by 18.9 g of 1-benzyl-4-piperidone in 100 ml of methanol. Then, 9.45 g sodium cyanoborohydride are added in portions while stirring at room temperature. After 72 hours the mixture is filtered, the residue dissolved in water and the solution made basic with 12.5% aqueous sodium hydroxide. It is extracted with methylene chloride, dried and evaporated to yield the 1-benzyl-4-(2-phenylaminoethylamino)-piperidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147786
出典データセットuspto-grants-1979_04
ORD IDord-e571c060f05d484fa41ce6089969dd32
出典メモuspto-grants-1979_04