反応式
N1([CH:10]=[O:11])C2C=CC=CC=2N=N1.FC(F)(F)C(O)=O.[N:19]1([C:25]2[N:33]=[C:32]([C:34]3[CH:35]=[N:36][C:37]([NH2:40])=[N:38][CH:39]=3)[N:31]=[C:30]3[C:26]=2[N:27]=[C:28]([N:46]2[CH2:51][CH2:50][NH:49][CH2:48][CH2:47]2)[N:29]3[CH2:41][C:42]([F:45])([F:44])[F:43])[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1>O1CCCC1.C(OCC)(=O)C>[NH2:40][C:37]1[N:36]=[CH:35][C:34]([C:32]2[N:31]=[C:30]3[C:26]([N:27]=[C:28]([N:46]4[CH2:47][CH2:48][N:49]([CH:10]=[O:11])[CH2:50][CH2:51]4)[N:29]3[CH2:41][C:42]([F:44])([F:43])[F:45])=[C:25]([N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[N:33]=2)=[CH:39][N:38]=1参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
Benzotriazole-1-carboaldehyde (55 mg, 0.38 mmol) was dissolved in tetrahydrofuran (10 ml) followed by the addition of 5-[6-morpholin-4-yl-8-piperazin-1-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl]pyrimidin-2-amine trifluoroacetate (200 mg, 0.29 mmol). The resulting mixture was stirred for 20 minutes and the reaction mixture was diluted with ethyl acetate, washed with 1 M sodium hydroxide and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography (chloroform:methanol=19:1) to give a white solid (80 mg, 56%).
後処理
- washwashed with 1 M sodium hydroxide and saturated brine
- dry with materialdried over magnesium sulfate
- customThe solvent was evaporated under reduced pressure
- customthe residue was purified by silica gel chromatography (chloroform:methanol=19:1)
出典と根拠
- ORDレコード
- ord-1f2504b763a54f5792290dba9c3f8777
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08097622B2
関連ノート
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