反応式
[C:1]1([N:7]=[C:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N-]=C=O.[NH2:13][C:14]1[N:19]([C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([NH2:26])[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:25]=[CH:24][CH:23]=[C:22]([NH:26][C:8]([NH:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[O:9])[CH:21]=2)[CH2:18][N:17]=[C:16]2[O:27][CH:28]=[CH:29][C:15]=12参加物
4
実験手順
The compound was prepared following the procedure described in Example 232(b), using phenyl isocyanate as the isocyanate of choice, and 4-Amino-3-(3-aminophenyl)furo[2,3-d]pyrimidine (10) as the diamine of choice. MS(ES) m/e 346 [M+H]+.
後処理
- customThe compound was prepared
出典と根拠
- ORDレコード
- ord-b37e47316bad4f80aff51432a3d6aa29
- 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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