Chlorosuccinimide → 3-[5-chloro-4-(2,4-difluoro-benzyloxy)-2-methyl-6-oxo-6H-pyrimidin-1-yl]-4-methyl-benzoic acid methyl ester
反応式
[CH3:1][O:2][C:3](=[O:29])[C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[C:6]([N:11]2[C:16](=[O:17])[CH:15]=[C:14]([O:18][CH2:19][C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][C:21]=3[F:27])[N:13]=[C:12]2[CH3:28])[CH:5]=1.[Cl:30]N1C(=O)CCC1=O>C(O)(C)C.ClC(Cl)C(O)=O>[CH3:1][O:2][C:3](=[O:29])[C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[C:6]([N:11]2[C:16](=[O:17])[C:15]([Cl:30])=[C:14]([O:18][CH2:19][C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][C:21]=3[F:27])[N:13]=[C:12]2[CH3:28])[CH:5]=1参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 60 °C
実験手順
To a solution of 3-[4-(2,4-difluoro-benzyloxy)-2-methyl-6-oxo-6H-pyrimidin-1-yl]-4-methyl-benzoic acid methyl ester from Example 1, Step A (260 mg, 0.65 mmol) in isopropanol (5 mL) was added N-chlorosuccinimide (95 mg, 0.71 mmol) and 3 drops of dichloroacetic acid. The solution was heated at 60° C. for three hours. The solution was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with water and brine and dried over magnesium sulfate. The slurry was filtered and concentrated to provide the chlorinated product as a light yellow semi-solid (230 mg, 82%). MS (M+H): 435
後処理
- concentrationThe solution was concentrated in vacuo
- customthe residue was partitioned between ethyl acetate and water
- washThe organic layer was washed with water and brine
- dry with materialdried over magnesium sulfate
- filtrationThe slurry was filtered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-015134128ec44ec29500c8eacc47b2ed
- 出典データセット
- uspto-grants-2015_06
- 特許番号
- US09056110B2
反応ノート
読み込み中…