化工社化工社 化学情報印刷レポート · 研究参考用
2-(cis-2,6-Dimethyl-1-piperidinyl)ethanamine → cis-(+/-)-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-alpha-methyl-2-oxo-1-pyrrolidineacetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(cis-2,6-Dimethyl-1-piperidinyl)ethanamine | HCID 783702 | — |
| 反応物 | Ethyl alpha-methyl-2-oxo-1-pyrrolidineacetate | HCID 15044021 | — |
| 生成物 | cis-(+/-)-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-alpha-methyl-2-oxo-1-pyrrolidineacetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04145347 |
| 出典データセット | uspto-grants-1979_03 |
| ORD ID | ord-e6aa23c201984e81bea970499bc5dd6f |
| 出典メモ | uspto-grants-1979_03 |