反応式
[NH2:1][C:2]1[N:7]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][CH3:15])=[CH:10][CH:9]=2)[CH2:6][N:5]=[C:4]2[S:16][CH:17]=[CH:18][C:3]=12.[F:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]([F:29])([F:28])[F:27])=[CH:22][C:21]=1[N:30]=[C:31]=[O:32].[N-]=C=O>>[NH2:1][C:2]1[N:7]([C:8]2[CH:9]=[CH:10][C:11]([N:14]([C:31]([NH:30][C:21]3[CH:22]=[C:23]([C:26]([F:27])([F:29])[F:28])[CH:24]=[CH:25][C:20]=3[F:19])=[O:32])[CH3:15])=[CH:12][CH:13]=2)[CH2:6][N:5]=[C:4]2[S:16][CH:17]=[CH:18][C:3]=12参加物
4
実験手順
The compound was prepared following the procedure described in Example 429, substituting 4-amino-3-(4-(methylamino)phenyl)-thieno[2,3-d]pyrimidine as the amine and using 2-fluoro-5-trifluoromethyl-phenyl isocyanate as the isocyanate of choice. MH+=462.
後処理
- customThe compound was prepared
出典と根拠
- ORDレコード
- ord-534534f0c63546078f699d706b25b0ca
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07427623B2
関連ノート
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