反応式
C(B(CC)[C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1)C.Br[C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH2:16].C(=O)([O-])[O-].[K+].[K+]>O.C(COC)OC.C(OCC)(=O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[N:6]1[CH:7]=[CH:8][CH:9]=[C:4]([C:13]2[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=2)[NH2:16])[CH:5]=1参加物
反応条件
- 温度
- 80 °C
実験手順
A mixture of diethyl 3-pyridylborane (16.3 g, 0.11 mol), 3-bromoaniline (12.2 ml, 0.11 mol), potassium carbonate (45.8 g, 0.33 mol) and tetrakis(triphenylphosphine)palladium(0) (80 mg) in a mixture of water (40 ml) and dimethoxyethane (80 ml) is heated to 80° C. under a stream of nitrogen over night. After cooling the mixture is diluted with water and ethyl acetate and filtered through a fluted filterpaper. The layers are separated. The aqueous layer is extracted once with ethyl acetate. The combined organic phases are dried over sodium sulfate and concentrated under reduced pressure. The residue is dissolved in ethanol. Water is added and the mixture is evaporated to dryness. This residue crystallizes upon trituration with ice-cold water. The crystals are collected, dried and washed with petroleum ether to afford pure 2p (16.3 g, 87%). Mp 75-76° C.
後処理
- temperatureAfter cooling the mixture
- filtrationfiltered through a fluted filterpaper
- customThe layers are separated
- extractionThe aqueous layer is extracted once with ethyl acetate
- dry with materialThe combined organic phases are dried over sodium sulfate
- concentrationconcentrated under reduced pressure
- dissolutionThe residue is dissolved in ethanol
- additionWater is added
- customthe mixture is evaporated to dryness
- customThis residue crystallizes upon trituration with ice-cold water
- customThe crystals are collected
- customdried
- washwashed with petroleum ether
出典と根拠
- ORDレコード
- ord-cc22c73af09b4ffa83cbfb8c9b647656
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06218547B1
関連ノート
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