Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2(1H)-Pyrimidinone, tetrahydro- → HCID 59586732, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2(1H)-Pyrimidinone, tetrahydro- | HCID 74615 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 1-Fluoro-2-isopropyl-4-nitrobenzene | HCID 59860488 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | HCID 59586732 | HCID 59586732 | — |
반응 단계
347 mg (3.47 mmol) of tetrahydropyrimidinone in 21 ml of DMSO are admixed at RT with 584 mg (5.21 mmol) of potassium tert-butoxide, and the mixture is stirred at RT for 45 min. 700 mg (3.82 mmol) of 1-fluoro-2-isopropyl-4-nitrobenzene are added and the mixture is stirred at 60° C. After 18 h, it is cooled and diluted with 250 ml of water. It is extracted three times with ethyl acetate and the combined organic phases are dried over sodium sulfate. After filtration, the solvents are removed under reduced pressure and the residue is purified by chromatography on silica gel (1:5→1:10 cyclohexane/ethyl acetate). This affords 140 mg (14% of theory) of the desired compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08198267B2 |
| 출처 데이터셋 | uspto-grants-2012_06 |
| ORD ID | ord-8a186f2eb15b422db9d30e34aaf3fc64 |
| 출처 메모 | uspto-grants-2012_06 |