(4-aminophenyl)-N-methylmethylenesulfonamide hydrochloride → CID 69598067
反応式
C(O[CH:4]=[C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([C:14]3[O:18][CH:17]=[N:16][CH:15]=3)[CH:12]=2)[NH:7][C:6]1=[O:19])C.Cl.[CH3:21][NH:22][S:23]([CH2:26][C:27]1[CH:32]=[CH:31][C:30]([NH2:33])=[CH:29][CH:28]=1)(=[O:25])=[O:24]>>[CH3:21][NH:22][S:23]([CH2:26][C:27]1[CH:32]=[CH:31][C:30]([NH:33][CH:4]=[C:5]2[C:13]3[C:8](=[CH:9][CH:10]=[C:11]([C:14]4[O:18][CH:17]=[N:16][CH:15]=4)[CH:12]=3)[NH:7][C:6]2=[O:19])=[CH:29][CH:28]=1)(=[O:24])=[O:25]参加物
3
実験手順
The title compound was prepared in 56% yield from ethoxymethylene-5-oxazol-5-yl-1,3-dihydro-indol-2-one and N-methyl-4-aminophenylmethanesulfonamide hydrochloride according to Procedure J: 1H NMR (DMSO-d6): δ 10.72 (d, 1H), 10.67 (s, 1H), 8.71 (d, 1H), 8.37 (s, 1H), 7.43–7.34 (m, 7H), 6.89 (m, 2H), 4.28 (s, 2H), 2.54 (d, 3H); APCI-MS m/z 409 (MH)−.
出典と根拠
- ORDレコード
- ord-24112a5c85a14c5cac70e55fbe1329f5
- 出典データセット
- uspto-grants-2006_09