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Azetidine → 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Azetidine | HCID 10422 | — |
| 反応物 | 4,6-Dichloro-5-pyrimidinecarbaldehyde | HCID 819691 | — |
| 触媒 | Triethylamine | HCID 8471 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde | HCID 86712562 | — |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829010B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-50b2e28456f84a5494615235ad31a5bc |
| 出典メモ | uspto-grants-2014_09 |