Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3,5-Dimethylpiperidine → 4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3,5-Dimethylpiperidine | HCID 118259 | — |
| 반응물 | 4-Chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine | HCID 59341120 | — |
| 생성물 | 4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine | HCID 57824685 | 84.7% |
반응 단계
0.2 g of 4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine and 0.32 g of 3,5-dimethylpiperidine (cis/trans=about 3/1) were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.23 g of 4-(3,5-dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine (hereinafter, referred to as Compound (11)). Compound (11) had the cis/trans diastereomer originated two methyls on the piperidine ring. The ratio of the cis/trans diastereomer was about 3.8/1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07732448B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-359178bc0bbb4b3da86334cd14e4f2bb |
| 출처 메모 | uspto-grants-2010_06 |