Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Potassium Iodide → DES(6-fluoro-1,2-benzoxazole)-2,4-difluorobenzoyl risperidone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 3-(2-Chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4hpyrido(1,2-a)pyrimidin-4-one | HCID 2763079 | — |
| 반응물 | (2,4-Difluorophenyl)(piperidin-4-yl)methanone hydrochloride | HCID 18759874 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | DES(6-fluoro-1,2-benzoxazole)-2,4-difluorobenzoyl risperidone | HCID 29941101 | — |
반응 단계
A suspension of 29.2 g (0.1116 mole) of 4-(2,4-difluoro-benzoyl)-piperidine-hydrochloride, 25.3 g (0.1117 mole) of 3-(2-chloroethyl)-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one, 500 ml of acetonitrile, 19.6 g (0.2333 mole) of sodium hydrogencarbonate and 0.25 g (0.0015 mole) of potassium iodide is heated to boiling for 10 hours with stirring. The reaction mixture is cooled to room temperature, to the residue 200 ml of water are added. The mixture is stirred for 30 minutes and extracted with 200 ml of dichloromethane. The organic phase is separated, dried over magnesium sulfate, filtered and the filtrate is evaporated. The oily residue thus obtained is purified as follows:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07307168B2 |
| 출처 데이터셋 | uspto-grants-2007_12 |
| ORD ID | ord-12fc39fc25a4411fbc84b164281c31d8 |
| 출처 메모 | uspto-grants-2007_12 |