참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(Trimethylsilyl)pyrrolidin-2-one | HCID 84461 | — |
| 반응물 | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | 3-(2-Chloropyrid 5-yl-methyl)-pyrrolid-2-one | HCID 18759788 | — |
반응 단계
Under a nitrogen atmosphere at a temperature of from −78° C. to −60° C., 180 ml of a 1.5 molar solution of lithium diisopropylamide (IDA) in cyclohexane are added dropwise to 31.4 g of N-trimethylsilylpyrrolid-2-one in 150 ml of tetrahydrofuran (THF) and the reaction mixture is stirred at the same temperature for a further one hour. Then, at from −78° C. to −60° C., 25.5 g of 2-chloro-5-chloromethylpyridine in 40 ml of THF are added, and the mixture is stirred for a further 16 hours at that temperature and then for a further three hours at room temperature. The reaction mixture is poured onto a mixture of ice/water and extracted with ethyl acetate, and the organic phase is separated off The ethyl acetate phase is dried over sodium sulfate and concentrated to dryness by evaporation in vacuo. The residue is purified on silica gel using ethyl acetate/hexane (7:1) as eluant. The title compound having a melting point of 117-118° C. (compound 1.3) is obtained
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06664248B2 |
|---|
| 출처 데이터셋 | uspto-grants-2003_12 |
|---|
| ORD ID | ord-dec8e6cd826940d6947cf8e1fe93d861 |
|---|
| 출처 메모 | uspto-grants-2003_12 |
|---|