Hydrochloric Acid → HCID 14990560、化合物
反応式
[NH2:1][C:2]1[CH:3]=[C:4]([C:12]([C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=2)=[O:13])[CH:5]=[CH:6][C:7]=1[NH:8][CH:9]([CH3:11])[CH3:10].Cl.[N:22]([O-])=O.[Na+].C(=O)([O-])[O-].[K+].[K+]>>[F:20][C:17]1[CH:16]=[CH:15][C:14]([C:12]([C:4]2[CH:5]=[CH:6][C:7]3[N:8]([CH:9]([CH3:10])[CH3:11])[N:22]=[N:1][C:2]=3[CH:3]=2)=[O:13])=[CH:19][CH:18]=1参加物
5
実験手順
To a stirred and cooled (5° C.) solution of 12.3 parts of [3-amino-4-[(1-methylethyl)amino]phenyl](4-fluorophenyl)methanone in 150 parts of a hydrochloric acid solution 6N were added 4.7 parts of sodium nitrite. Upon complete addition, stirring was continued for 1 hour at room temperature. The mixture was treated with a potassium carbonate solution to pH 9 and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated, yielding 17 parts (100%) of (4-fluorophenyl) [1-(1-methylethyl)-1H-benzotriazol-5-yl]methanone as a residue (int. 3).
後処理
- additionUpon complete addition
- stirringstirring
- extractionthe product was extracted with dichloromethane
- customThe extract was dried
- filtrationfiltered
- customevaporated
出典と根拠
- ORDレコード
- ord-64722818d6794fb993585eec258a4382
- 出典データセット
- uspto-grants-1990_07
- 特許番号
- US04943574
反応ノート
読み込み中…