1H-Pyrazole-3-carbaldehyde → HCID 178477654、化合物

HRID 13338

反応式

HRID 13338 の反応式
[F:1][C:2]1[CH:28]=[CH:27][CH:26]=[C:25]([F:29])[C:3]=1[O:4][C:5]1[CH:10]=[C:9]([O:11][C:12]2[CH:13]=[N:14][C:15]([S:18]([CH2:21][CH3:22])(=[O:20])=[O:19])=[CH:16][CH:17]=2)[CH:8]=[C:7]([NH2:23])[C:6]=1[NH2:24].[NH:30]1[CH:34]=[CH:33][C:32]([CH:35]=O)=[N:31]1>>[F:29][C:25]1[CH:26]=[CH:27][CH:28]=[C:2]([F:1])[C:3]=1[O:4][C:5]1[C:6]2[N:24]=[C:35]([C:32]3[CH:33]=[CH:34][NH:30][N:31]=3)[NH:23][C:7]=2[CH:8]=[C:9]([O:11][C:12]2[CH:13]=[N:14][C:15]([S:18]([CH2:21][CH3:22])(=[O:20])=[O:19])=[CH:16][CH:17]=2)[CH:10]=1

参加物

3

反応物 2

HCID 122183831H-Pyrazole-3-carbaldehydeHCID 231452173-(2,6-Difluoro-phenoxy)-5-(6-ethanesulfonyl-pyridin-3-yloxy)-benzene-1,2-diamine

生成物 1

HCID 178477654HCID 178477654、化合物

実験手順

The entitled compound was obtained in the same method as in Example 202 or in accordance with the method or by combining it with an ordinary method but using 3-(2,6-difluoro-phenoxy)-5-(6-ethanesulfonyl-pyridin-3-yloxy)-benzene-1,2-diamine obtained in Example 268 and 1H-pyrazole-3-carboxaldehyde.

後処理

  1. customThe entitled compound was obtained in the same method as in Example 202 or in accordance with the method

出典と根拠

ORDレコード
ord-90b7e6a06e6f4d72bedc0f4a4ab8edad
出典データセット
uspto-grants-2010_06
特許番号
US07728025B2

関連ノート

読み込み中…