1-Methyl-3-hydroxypyridine-2-one → 5-(1-Methyl-2-oxo-1,2-dihydro-pyridin-3-yloxy)-6-(4-methanesulfonyl-phenoxy)-2-pyridin-2-yl-1H-benzimidazole

HRID 13337

反応式

HRID 13337 の反応式
C(OC([C:6]1[CH:38]=[CH:37]C=C[C:7]=1[O:8][C:9]1[C:23]([O:24][C:25]2[CH:30]=[CH:29][C:28]([S:31]([CH3:34])(=[O:33])=[O:32])=[CH:27][CH:26]=2)=[CH:22][C:12]2[NH:13][C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=3)=[N:15][C:11]=2[CH:10]=1)=O)C.[CH3:39][N:40]1C=CC=C(O)[C:41]1=[O:47]>>[CH3:39][N:40]1[CH:37]=[CH:38][CH:6]=[C:7]([O:8][C:9]2[C:23]([O:24][C:25]3[CH:26]=[CH:27][C:28]([S:31]([CH3:34])(=[O:33])=[O:32])=[CH:29][CH:30]=3)=[CH:22][C:12]3[NH:13][C:14]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=4)=[N:15][C:11]=3[CH:10]=2)[C:41]1=[O:47]

参加物

3

反応物 2

HCID 880261-Methyl-3-hydroxypyridine-2-oneHCID 231451405-(2-Ethoxycarbonyl-phenoxy)-6-(4-methanesulfonyl-phenoxy)-2-pyridin-2-yl-1H-benzimidazole

生成物 1

HCID 231453955-(1-Methyl-2-oxo-1,2-dihydro-pyridin-3-yloxy)-6-(4-methanesulfonyl-phenoxy)-2-pyridin-2-yl-1H-benzimidazole

実験手順

The entitled compound was obtained as a brown solid in the same method as in Example 14 or in accordance with the method or by combining it with an ordinary method but using 5-fluoro-4-(4-methanesulfonyl-phenoxy)-2-nitro-phenylamine obtained in Example 14 and 1-methyl-2-oxo-1,2-dihydro-pyridin-3-ol.

後処理

  1. customThe entitled compound was obtained as a brown solid in the same method as in Example 14 or in accordance with the method

出典と根拠

ORDレコード
ord-3b99a0b0c8f64e1e85c662db1bbbab56
出典データセット
uspto-grants-2010_06
特許番号
US07728025B2

関連ノート

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