Sodium Hydroxide → N-[4-(2,2-difluoroethyl)oxy-3-hydroxycarbonyl-phenyl]-2-chloro-5-(tert-butylcarbonylamino)methyl-benzamide
反応式
[F:1][CH:2]([F:34])[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:28])[C:13]2[CH:18]=[C:17]([CH2:19][NH:20][C:21]([C:23]([CH3:26])([CH3:25])[CH3:24])=[O:22])[CH:16]=[CH:15][C:14]=2[Cl:27])=[CH:7][C:6]=1[C:29]([O:31]CC)=[O:30].[OH-].[Na+]>CCO>[F:34][CH:2]([F:1])[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:28])[C:13]2[CH:18]=[C:17]([CH2:19][NH:20][C:21]([C:23]([CH3:26])([CH3:25])[CH3:24])=[O:22])[CH:16]=[CH:15][C:14]=2[Cl:27])=[CH:7][C:6]=1[C:29]([OH:31])=[O:30]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of N-[4-(2,2-difluoroethyl)oxy-3-ethoxycarbonyl-phenyl]-2-chloro-5-(tert-butylcarbonylamino)methyl-benzamide (0.470 mg, 0.946 mmol) and 1.4 mL 2M NaOH in 5.0 mL EtOH was stirred at rt for 3 h and concentrated i.vac. Water was added and it was acidified with 2 M HCl. The resulting precipitate was filtered, washed with water and dried. Yield: (86%). MS [M+H]+=469 (Cl isotope pattern); TLC: Rf=0.25 (silica gel, DCM:EtOH 9:1).
後処理
- concentrationconcentrated i.vac
- additionWater was added
- filtrationThe resulting precipitate was filtered
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-8a22831937c947078c14f585e14c31c0
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08951999B2
反応ノート
読み込み中…