反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[N:10]=[C:11]=[O:12].[N-:13]=C=O.[NH2:16][C:17]1[N:22]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25](N)[CH:24]=2)[CH2:21][N:20]=[C:19]2[O:30][CH:31]=[CH:32][C:18]=12>>[NH2:16][C:17]1[N:22]([C:23]2[CH:28]=[CH:27][C:26]([N:10]([C:3]3[CH:4]=[C:5]([O:8][CH3:9])[CH:6]=[CH:7][C:2]=3[F:1])[C:11]([NH2:13])=[O:12])=[CH:25][CH:24]=2)[CH2:21][N:20]=[C:19]2[O:30][CH:31]=[CH:32][C:18]=12参加物
4
実験手順
The compound was prepared following the procedure described in Example 232(b), using 2-fluoro-5-methoxyphenyl 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 394 [M+H]+.
後処理
- customThe compound was prepared
出典と根拠
- ORDレコード
- ord-6b5fd8f9879e4964b2d6dcae9287a2f7
- 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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