3-Formyl-2-methylindole → 3-(2-Methyl-1H-indol-3-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide

反応式

[NH2:1][S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=[O:14])[CH2:8]2)(=[O:4])=[O:3].[CH3:15][C:16]1[NH:17][C:18]2[C:23]([C:24]=1[CH:25]=O)=[CH:22][CH:21]=[CH:20][CH:19]=2>>[CH3:15][C:16]1[NH:17][C:18]2[C:23]([C:24]=1[CH:25]=[C:8]1[C:7]3[C:11](=[CH:12][CH:13]=[C:5]([S:2]([NH2:1])(=[O:4])=[O:3])[CH:6]=3)[NH:10][C:9]1=[O:14])=[CH:22][CH:21]=[CH:20][CH:19]=2

参加物

反応物 2

HCID 731663-Formyl-2-methylindole

HCID 101982322-Oxoindoline-5-sulfonamide

生成物 1

HCID 693448633-(2-Methyl-1H-indol-3-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide

実験手順

5-Aminosulfonyl-2-oxindole was condensed with 2-methylindole-3-carboxaldehyde to give the title compound.

出典と根拠

ORDレコード: ord-e513d9d542a6480d8480ffa4bf363cc1
出典データセット: uspto-grants-2004_03
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US06706709B2

反応ノート

読み込み中…