化工社化工社 化学情報印刷レポート · 研究参考用
Potassium Fluoride → 5-[2-(methyloxy)-3-pyridinyl]-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | (2-Methoxypyridin-3-yl)boronic acid | HCID 2762709 | — |
| 反応物 | 5-iodo-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione | HCID 67519719 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-[2-(methyloxy)-3-pyridinyl]-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione | HCID 24759550 | — |
反応手順
5-Iodo-1-{3-[(1S,5R)-1-(4-trifluoromethyl-phenyl)-3-aza-bicyclo[3.1.0]hex-3-yl]-propyl}-1H-pyrimidine-2,4-dione (Prep40, 150 mg, 0.3 mmol) was dissolved in degassed MeOH (4 mL). 2-Methoxy-pyridine-3-boronic acid (136 mg, 0.9 mmol), KF (155 mg, 2.7 mmol), and Pd(OAc)2 (15 mg, 10% weight) were added and the mixture was heated to vigorous reflux for 2.5 hours. The mixture was diluted with MeOH, loaded on SCX cartridge washing with MeOH and MeOH/NH3 95:5. The solvent was evaporated under vacuum and the residue was purified by flash chromatography with ethyl acetate to give the title compound as free base (70 mg, 48% 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-6a3ad0ac470e46af8d3f533493a1a0dd |
| 出典メモ | uspto-grants-2010_06 |