Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 4-Oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butyric acid methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Butanoic acid, 4-chloro-4-oxo-, methyl ester | HCID 73888 | — |
| 반응물 | 1-(3-Aminopropyl)-2-pyrrolidinone | HCID 82111 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butyric acid methyl ester | HCID 53970243 | 88.3% |
반응 단계
To a solution of 1-(3-aminopropyl)-2-oxopyrrolidine (570 mg) in methylene chloride (10 ml) were added triethylamine (0.67 ml) and 3-carbomethoxy propionylchloride (600 mg) in sequence under ice-cooling and the mixture was stirred for 0.5 hour. After 3.5 hours' stirring at room temperature, the reaction mixture was poured into ice water and extracted with chloroform. The organic layer was washed with 1N hydrochloric acid, a saturated aqueous solution of sodium bicarbonate and saturated brine in sequence, and dried over magnesium sulfate, followed by concentration. The residue was purified by silica gel column chromatography (chloroform-methanol) to give 902 mg of 4-oxo-4-[3-(2-oxo-1-pyrrolidinyl)propylamino]butyric acid methyl ester.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05118811 |
| 출처 데이터셋 | uspto-grants-1992_06 |
| ORD ID | ord-5817a10d96c4487e991cfff161e5aa83 |
| 출처 메모 | uspto-grants-1992_06 |