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Ammonia → 2-(4-Chlorophenyl)-3-(2-oxo-1-pyrrolidinylmethyl)-6-methylimidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 2-Pyrrolidinone, 1-(hydroxymethyl)- | HCID 84911 | — |
| 反応物 | 2-(4-Chlorophenyl)-6-methylimidazo[1,2-a]pyridine | HCID 735911 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-(4-Chlorophenyl)-3-(2-oxo-1-pyrrolidinylmethyl)-6-methylimidazo[1,2-a]pyridine | HCID 13589601 | — |
反応手順
An intimate mixture is prepared of 4.8 g (0.02 mol) of 2-(4-chlorophenyl)-6-methylimidazo[1,2-a]pyridine and 2.53 g (0.022 mol) of N-hydroxymethyl-2-pyrrolidinone, and this is then introduced into 20 ml of concentrated sulphuric acid. The solution is stirred for one day at room temperature, then poured into 800 ml of water, and 55 ml of ammonia solution are added. The lactam is extracted with methylene chloride, the organic phase is washed, dried and evaporated, and the residue is purified by chromatography, eluting with a 70:30 ethyl acetate, toluene mixture. The white solid obtained melts at 186°-187.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04650796 |
| 出典データセット | uspto-grants-1987_03 |
| ORD ID | ord-d734378739904929b8c1d367de515346 |
| 出典メモ | uspto-grants-1987_03 |