反応式
[CH3:1][C:2]1[N:3]=[C:4]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[S:5][C:6]=1[C:7]([OH:9])=O.[N:16]1([C:22]2[N:27]=[CH:26][C:25]([NH2:28])=[CH:24][CH:23]=2)[CH2:21][CH2:20][O:19][CH2:18][CH2:17]1>>[N:16]1([C:22]2[N:27]=[CH:26][C:25]([NH:28][C:7]([C:6]3[S:5][C:4]([C:10]4[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=4)=[N:3][C:2]=3[CH3:1])=[O:9])=[CH:24][CH:23]=2)[CH2:21][CH2:20][O:19][CH2:18][CH2:17]1参加物
3
実験手順
With a procedure similar to example 1 above, 4-methyl-2-phenyl-thiazole-5-carboxylic acid (6-morpholin-4-yl-pyridin-3-yl)-amide was prepared from 4-methyl-2-phenyl-thiazole-5-carboxylic acid and 6-morpholin-4-yl-pyridin-3-ylamine. LCMS calcd for C20H20N4O2S (m/e) 380, obsd 381 (M+H).
出典と根拠
- ORDレコード
- ord-b28739cb00b940179813dcd148105654
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07714126B2
関連ノート
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