反応式
NC1[CH:3]=[C:4](B(O)O)[CH:5]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:7]=1.[C:15](=O)([O-])[O-].[K+].[K+]>C1(C)C(CCO)=CC=CC=1>[CH3:15][CH2:11][O:10][C:8]([CH3:6])=[O:9].[CH3:3][CH2:4][CH2:5][CH:6]([CH3:8])[CH3:7]参加物
4
反応条件
- 温度
- 90 °C
実験手順
A mixture of 3-amino-5-methoxycarbonylphenylboronic acid (161 mg, 0.82 mmol), Pd(0) [PPh3]4 (50 mg, 5 mol %), potassium carbonate (905 mg, 6.6 mmol) and 2-(2-benzyloxy-5-chloro)phenyl-1-bromocyclopent-1-ene (298 mg, 0.82 mmol) in toluene-ethanol (1:1 10 mL) were stirred at 90° C., under nitrogen, for 2 hrs. After cooling the reaction mixture was poured onto water (10 ml) and extracted with diethyl ether (2×10 ml). The combined extracts were dried and evaporated. Flash chromatography [EtOAc/Iso-hexane 5:95-1:4] gave the product as a yellow oil 200 mg 56% LC/MS: Rt=4.00 [M+H] 434 (1 Cl)
後処理
- temperatureAfter cooling the reaction mixture
- additionwas poured onto water (10 ml)
- extractionextracted with diethyl ether (2×10 ml)
- customThe combined extracts were dried
- customevaporated
出典と根拠
- ORDレコード
- ord-68ffa633470f43cc820eaf9a35d52571
- 出典データセット
- uspto-grants-2007_06
- 特許番号
- US07232821B2
関連ノート
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