反応式
[C:1]1([C:7]2([C:10](Cl)=[O:11])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:13][C:14]1[N:19]([C:20]2[CH:25]=[CH:24][C:23]([NH2:26])=[CH:22][CH:21]=2)[CH2:18][N:17]=[C:16]2[O:27][CH:28]=[CH:29][C:15]=12>>[NH2:13][C:14]1[N:19]([C:20]2[CH:21]=[CH:22][C:23]([NH:26][C:10]([C:7]3([C:1]4[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=4)[CH2:9][CH2:8]3)=[O:11])=[CH:24][CH:25]=2)[CH2:18][N:17]=[C:16]2[O:27][CH:28]=[CH:29][C:15]=12参加物
3
実験手順
The compound was prepared following the procedure described in Example 474, using 1-Phenyl-cyclopropanecarbonyl chloride as the acid chloride of choice, and 4-Amino-3-(4-aminophenyl)furo[2,3-d]pyrimidine (9) as the diamine of choice. MS(ES) m/e 371 [M+H]+.
後処理
- customThe compound was prepared
出典と根拠
- ORDレコード
- ord-99996d2b94e744c586e2763bf5b7c568
- 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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