化工社化工社 化学情報印刷レポート · 研究参考用
Sodium Carbonate → 5-(2-Chloro-6-methyl-pyridin-3-yl)-2,4-dimethoxy-pyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | 5-Iodo-2,4-dimethoxypyrimidine | HCID 263416 | — |
| 反応物 | 2-Chloro-6-methylpyridine-3-boronic acid | HCID 2763127 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | 1-Propanol | HCID 1031 | — |
| 生成物 | 5-(2-Chloro-6-methyl-pyridin-3-yl)-2,4-dimethoxy-pyrimidine | HCID 58994217 | — |
反応手順
2,4-Dimethoxy-5-iodopyrimidine (957 mg, 3.59 mmol) was dissolved in degassed n-PrOH (18 ml) and then 2-chloro-6-methylpyridine-3-boronic acid (923 mg, 5.39 mmol), Na2CO3 (761 mg, 7.2 mmol), PPh3 (94 mg, 0.35 mmol) and Pd(OAc)2 (40 mg) were added. The suspension was stirred at reflux for 3 hours. The solvent was evaporated under vacuum and the crude was partitioned between water and DCM. The organic phase was dried (Na2SO4) and evaporated to give the title compound that was used without further purification in the next step (quantitative yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07727988B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-a4c85c3e9498464ba3062577b6f704f4 |
| 出典メモ | uspto-grants-2010_06 |