1,2-Dichloroethane → HCID 10412743、化合物
反応式
[N+:1]([C:4]1[C:9]2[S:10][C:11]([C:13]([OH:15])=O)=[CH:12][C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.[NH2:30][C:31]1[C:32]([O:46][CH3:47])=[C:33]([NH:41][S:42]([CH3:45])(=[O:44])=[O:43])[CH:34]=[C:35]([C:37]([CH3:40])([CH3:39])[CH3:38])[CH:36]=1>CN(C=O)C>[C:37]([C:35]1[CH:34]=[C:33]([NH:41][S:42]([CH3:45])(=[O:44])=[O:43])[C:32]([O:46][CH3:47])=[C:31]([NH:30][C:13]([C:11]2[S:10][C:9]3[C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=[CH:7][C:8]=3[CH:12]=2)=[O:15])[CH:36]=1)([CH3:40])([CH3:38])[CH3:39]参加物
6
実験手順
To a solution of the above carboxylic acid (900 mg) in DMF was added EDC (1.2 eq) and HOBT (1.2 eq). After stirring for 10 min, N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide (1.0 eq) was added. The suspension was stirred at room temperature for 48 h. The DMF was removed in vacuo and the resulting oil was dissolved in EtOAc, washed with water three times, followed by saturated NaHCO3 solution and brine. The organics were dried over MgSO4, filtered and concentrated to give a crude yellow solid which was triturated with 30% EtOAc/hex (small amount) and filtered to provide 7-nitro-benzo[b]thiophene-2-carboxylic acid (5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-amide as a bright yellow solid (1.4 g, 72%).
後処理
- stirringThe suspension was stirred at room temperature for 48 h
- customThe DMF was removed in vacuo
- dissolutionthe resulting oil was dissolved in EtOAc
- washwashed with water three times
- dry with materialThe organics were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customto give a crude yellow solid which
- customwas triturated with 30% EtOAc/hex (small amount)
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-ed110744363446d0b3ef6cf5da8fdbff
- 出典データセット
- uspto-grants-2009_06
- 特許番号
- US07550461B2
反応ノート
読み込み中…