反応式
[OH:1][C:2]1[C:3](I)=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1.C([O-])(=O)C.[K+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:34]([O:38][CH2:39][CH3:40])(=[O:37])[CH:35]=[CH2:36]>CN(C=O)C.O.[Pd](Cl)Cl>[OH:1][C:2]1[C:3]([C:35](=[CH2:36])[C:34]([O:38][CH2:39][CH3:40])=[O:37])=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1参加物
8
反応条件
- 温度
- 120 °C
実験手順
To a solution of 3-hydroxy-2-iodo-6-methylpyridine (1.175 g, 5.0 mmol) in DMF (9.5 ml) and water (0.5 ml) were added potassium acetate (1.23 g, 12.5 mmol), triphenylphosphine (105 mg, 0.40 mmol), palladium chloride (36 mg, 0.20 mmol) and ethyl acrylate (1.63 ml, 1.50 g, 15.0 mmol). The mixture was placed under nitrogen and heated at 120° C. for 1.5 h. The mixture was cooled, filtered from deposited palladium black, and added to water (100 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (2×25 ml) and with brine (25 ml), then dried over sodium sulphate and evaporated. This left a tan solid, the product (951 mg, 91%). mp 192°-195° C. (dec)
後処理
- temperatureThe mixture was cooled
- filtrationfiltered
- additionadded to water (100 ml)
- extractionThe product was extracted into ethyl acetate (3×30 ml)
- washThe combined extracts were washed with water (2×25 ml) and with brine (25 ml)
- dry with materialdried over sodium sulphate
- customevaporated
- waitThis left a tan solid
出典と根拠
- ORDレコード
- ord-daea2679130c4e96a69efc91647c4537
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05726315
関連ノート
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