Triethylamine → HCID 59152162、化合物
反応式
[C:1]([N:5]1[C:9]([NH:10][C:11]2[CH:16]=[N:15][CH:14]=[C:13](Cl)[N:12]=2)=[CH:8][CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].[CH:18]([B-](F)(F)F)=[CH2:19].[K+].C(N(CC)CC)C>C(O)CC>[C:1]([N:5]1[C:9]([NH:10][C:11]2[CH:16]=[N:15][CH:14]=[C:13]([CH:18]=[CH2:19])[N:12]=2)=[CH:8][CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2]参加物
反応条件
- 温度
- 110 °C
実験手順
A mixture of 65.04 g of N-(1-tert-butyl-1H-pyrazol-5-yl)-6-chloropyrazin-2-amine, 41.6 g of potassium vinyltrifluoroborate, 4.22 g of (1,1′-bis (diphenylphosphino)ferrocene)dichloropalladium(II) dichloromethane complex, 72 ml of triethylamine and 685 ml of 1-propanol was stirred at 110° C. overnight, followed by cooling down to room temperature and concentrated in vacuo. The obtained residue was diluted with ethyl acetate, and an insoluble matter was filtered off using Celite. The resulting ethyl acetate solution was washed with water, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo. The obtained residue was suspended in 100 ml of ethyl acetate, and 400 ml of diisopropylether was added to the mixture. The obtained precipitate was collected to give the title compound as a pale brown solid.
後処理
- temperatureby cooling down to room temperature
- concentrationconcentrated in vacuo
- additionThe obtained residue was diluted with ethyl acetate
- filtrationan insoluble matter was filtered off
- washThe resulting ethyl acetate solution was washed with water
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated in vacuo
- addition400 ml of diisopropylether was added to the mixture
- customThe obtained precipitate was collected
出典と根拠
- ORDレコード
- ord-796fb5c675cc485293f5af6b0cf0d8dd
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07915263B2
反応ノート
読み込み中…