Benzo(d)thiazol-2-amine → tert-butyl 8-(benzo[d]thiazol-2-ylcarbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
反応式
[C:1]([O:5][C:6]([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[C:11]([C:18](O)=[O:19])[CH:12]=[CH:13][CH:14]=2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[S:21]1[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[N:23]=[C:22]1[NH2:30].Cl.C(N=C=NCCCN(C)C)C>CN(C)C1C=CN=CC=1.ClCCl>[S:21]1[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[N:23]=[C:22]1[NH:30][C:18]([C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:10]=1[CH2:9][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[CH2:17][CH2:16]2)=[O:19]参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-8-carboxylic acid (6.7 g), benzo[d]thiazol-2-amine (5.5 g) and 4-dimethylaminopyridine (6.6 g) in dichloromethane (78 mL) were treated with 1-ethyl-3-[3-(dimethylamino)propyl]-carbodiimide hydrochloride (9.3 g) at room temperature overnight. The reaction mixture was diluted with dichloromethane (450 mL) and washed with 3% aqueous HCl, water, and brine. The organic layer was dried over Na2SO4, filtered and concentrated to provide the title compound.
後処理
- washwashed with 3% aqueous HCl, water, and brine
- dry with materialThe organic layer was dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-581d648b006f48cc802c7346f9ebf4dd
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08883784B2
反応ノート
読み込み中…