反応式
CC(C)([O:4][C:5]1[N:10]=[C:9]([O:11]C(C)(C)C)[C:8]([C:16]2(O)[C:22]3[N:23]=[C:24]([CH3:26])[O:25][C:21]=3[CH2:20][CH2:19][C:18]3[CH:27]=[C:28]([CH2:31][CH3:32])[CH:29]=[CH:30][C:17]2=3)=[CH:7][N:6]=1)C.C([SiH](CC)CC)C.B(F)(F)F.CCOCC.C(=O)(O)[O-].[Na+]>ClCCl>[CH2:31]([C:28]1[CH:29]=[CH:30][C:17]2[CH:16]([C:8]3[C:9](=[O:11])[NH:10][C:5](=[O:4])[NH:6][CH:7]=3)[C:22]3[N:23]=[C:24]([CH3:26])[O:25][C:21]=3[CH2:20][CH2:19][C:18]=2[CH:27]=1)[CH3:32]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 0 °C
実験手順
A stirred solution of the product from step (i) (0.60 g) in dichloromethane (15 ml) was treated with triethylsilane (0.225 ml) and cooled to 0° C. Boron trifluoride etherate (0.65 ml) was added in four equal portions at 5 minute intervals and the reaction stirred at room temperature for 16 hours. The reaction was poured into saturated sodium bicarbonate solution (200 ml) and extracted with ethyl acetate. The extracts were dried (MgSO4) and evaporated to give a yellow solid which was purified by reverse phase chromatography eluting with 50% to 80% methanol in 0.1% aqueous ammonium acetate.
後処理
- extractionextracted with ethyl acetate
- dry with materialThe extracts were dried (MgSO4)
- customevaporated
- customto give a yellow solid which
- customwas purified by reverse phase chromatography
- washeluting with 50% to 80% methanol in 0.1% aqueous ammonium acetate
出典と根拠
- ORDレコード
- ord-81e57e3676454468b17fdd38b48e4ab2
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06218376B1
関連ノート
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