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HRID 614484作成日:2026年10月24日

2-(cis-2,6-Dimethyl-1-piperidinyl)ethanamine → cis-(+/-)-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-alpha-methyl-2-oxo-1-pyrrolidineacetamide

https://huagongshe.com/ja/reaction/614484

反応式

関与物質

役割名称HCID仕込み量
反応物2-(cis-2,6-Dimethyl-1-piperidinyl)ethanamineHCID 783702—
反応物Ethyl alpha-methyl-2-oxo-1-pyrrolidineacetateHCID 15044021—
生成物cis-(+/-)-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-alpha-methyl-2-oxo-1-pyrrolidineacetamideHCID 22807214—

反応手順

A mixture of 9.25 g. of ethyl α-methyl-2-oxo-1-pyrrolidineacetate (British Pat. No. 1,309,692) and 11.2 g. of cis-2-(2,6-dimethyl-1-piperidinyl)ethylamine is heated under nitrogen and an air condenser plugged with cotton for 20 hours at 150° C. The excess cis-2-(2,6-dimethyl-1-piperidinyl)ethylamine is evaporated at reduced pressure and the residue is fractionated. The product, cis-(±)-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-α-methyl-2-oxo-1-pyrrolidineacetamide, is obtained as an oil, b.p. 168°-170° C./0.1 mm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04145347
出典データセットuspto-grants-1979_03
ORD IDord-e6aa23c201984e81bea970499bc5dd6f
出典メモuspto-grants-1979_03