Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonia → 2-(4-Chlorophenyl)-3-(2-oxo-1-pyrrolidinylmethyl)-6-methylimidazo[1,2-a]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 2-Pyrrolidinone, 1-(hydroxymethyl)- | HCID 84911 | — |
| 반응물 | 2-(4-Chlorophenyl)-6-methylimidazo[1,2-a]pyridine | HCID 735911 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(4-Chlorophenyl)-3-(2-oxo-1-pyrrolidinylmethyl)-6-methylimidazo[1,2-a]pyridine | HCID 13589601 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04650796 |
| 출처 데이터셋 | uspto-grants-1987_03 |
| ORD ID | ord-d734378739904929b8c1d367de515346 |
| 출처 메모 | uspto-grants-1987_03 |