Diisopropylethylamine → Ethyl {2-methyl-4-[(propyl{4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)methyl]phenoxy}acetate
反応式
[CH3:1][C:2]1[CH:14]=[C:13]([CH2:15][NH:16][CH2:17][CH2:18][CH3:19])[CH:12]=[CH:11][C:3]=1[O:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7].C(N(CC)C(C)C)(C)C.CS([C:33]1[N:38]=[C:37]([C:39]2[CH:44]=[CH:43][C:42]([C:45]([F:48])([F:47])[F:46])=[CH:41][CH:40]=2)[CH:36]=[CH:35][N:34]=1)(=O)=O>C(Cl)Cl>[CH3:1][C:2]1[CH:14]=[C:13]([CH2:15][N:16]([CH2:17][CH2:18][CH3:19])[C:33]2[N:38]=[C:37]([C:39]3[CH:40]=[CH:41][C:42]([C:45]([F:48])([F:46])[F:47])=[CH:43][CH:44]=3)[CH:36]=[CH:35][N:34]=2)[CH:12]=[CH:11][C:3]=1[O:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a mixture of ethyl {2-methyl-4-[(propylamino)methyl]phenoxy}acetate (652 mg, 2.46 mmol) and N,N-diisopropylethylamine (570 μL, 3.28 mmol) was added 2-(methylsulfonyl)-4-[4-(trifluoromethyl)phenyl]pyrimidine (495 mg, 1.64 mmol) and the resultant mixture heated at 100° C. for 16 h in a reactivial. The cooled reaction mixture was diluted with CH2Cl2 (30 mL), washed with water (20 mL), the aqueous extracted with CH2Cl2 (30 mL) and the CH2Cl2 extracts combined and the solvent removed in vacuo. Purification by Biotage™ chromatography (silica, 90 g) eluted with cyclohexane:EtOAc 10:1 afforded the title compound as a colourless gum (139 mg).
後処理
- customThe cooled reaction mixture
- washwashed with water (20 mL)
- extractionthe aqueous extracted with CH2Cl2 (30 mL)
- customthe solvent removed in vacuo
- customPurification by Biotage™ chromatography (silica, 90 g)
- washeluted with cyclohexane:EtOAc 10:1
出典と根拠
- ORDレコード
- ord-058f92e9dbd046b084f39d0f0e9e1b85
- 出典データセット
- uspto-grants-2007_04
- 特許番号
- US07199239B2
反応ノート
読み込み中…