Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Azetidine → 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Azetidine | HCID 10422 | — |
| 반응물 | 4,6-Dichloro-5-pyrimidinecarbaldehyde | HCID 819691 | — |
| 촉매 | Triethylamine | HCID 8471 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde | HCID 86712562 | — |
반응 단계
To a solution of 4,6-dichloropyrimidine-5-carbaldehyde (1.00 g, 5.65 mmol) in chloroform at 0° C. were added azetidine (99%, 0.392 mL, 5.71 mmol) and triethylamine (5 drops). The reaction mixture was allowed to warm to room temperature and then stirred for 18 hours. The reaction mixture was filtered, and the filtrate was purified by silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) to provide the product. Yield: 880 mg, 4.45 mmol, 79%. LCMS m/z 198.1, 200.1 (M+1). 1H NMR (400 MHz, CD3OD) δ 2.34-2.43 (m, 2H), 4.12-4.33 (br m, 4H), 8.30 (s, 1H), 10.28 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08829010B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-50b2e28456f84a5494615235ad31a5bc |
| 출처 메모 | uspto-grants-2014_09 |