反応式
[F:1][C:2]1[CH:23]=[CH:22][C:5]([CH2:6][CH2:7][C:8]2[S:9][C:10]3[N:11]=[C:12]([NH2:21])[N:13]=[C:14](S(C)(=O)=O)[C:15]=3[N:16]=2)=[CH:4][CH:3]=1.[CH3:24][O:25][C:26]1[CH:36]=[CH:35][C:29]([O:30][CH2:31][C:32]([OH:34])=O)=[CH:28][CH:27]=1.CN(C(O[N:45]1N=[N:52][C:47]2C=CC=C[C:46]1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[CH3:59][CH2:60]N(C(C)C)C(C)C>CN(C=O)C.O>[NH2:21][C:12]1[N:13]=[C:14]([N:45]2[CH2:46][CH2:47][N:52]([C:32](=[O:34])[CH2:31][O:30][C:29]3[CH:28]=[CH:27][C:26]([O:25][CH3:24])=[CH:36][CH:35]=3)[CH2:60][CH2:59]2)[C:15]2[N:16]=[C:8]([CH2:7][CH2:6][C:5]3[CH:22]=[CH:23][C:2]([F:1])=[CH:3][CH:4]=3)[S:9][C:10]=2[N:11]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 2-(4-fluorophenethyl)-7-(methylsulfonyl)thiazolo[5,4-d]pyrimidin-5-amine (40 mg, 0.11 mmol) and 4-methoxyphenoxyacetic acid (30 mg, 0.17 mmol) in DMF (2 ml) was added TBTU (N,N,N′,N′-tetramethyl-O-(benzotriazol-1-yl)uronium tetrafluoroborate, 54 mg, 0.17 mmol), followed by DIPEA (29 μl, 0.17 mmol. The reaction mixture was stirred at room temperature for 3 hours. The mixture was diluted with water and extracted with dichloromethane. The combined organic layers were washed with brine and dried over Na2SO4. After removing the solvents under reduced pressure, the crude residue was purified by flash chromatography on silica (CH2Cl2/MeOH 40:1), yielding the title compound as a white solid (40 mg, 69%).
後処理
- extractionextracted with dichloromethane
- washThe combined organic layers were washed with brine
- dry with materialdried over Na2SO4
- customAfter removing the solvents under reduced pressure
- customthe crude residue was purified by flash chromatography on silica (CH2Cl2/MeOH 40:1)
出典と根拠
- ORDレコード
- ord-dd466f73392440a6a5c0bb1776838d2f
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09193741B2
関連ノート
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