반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[C:9]1([C:12](Cl)=[O:13])[CH2:11][CH2:10]1.[NH2:15][C:16]1[N:21]([C:22]2[CH:27]=[CH:26][C:25]([NH2:28])=[CH:24][CH:23]=2)[CH2:20][N:19]=[C:18]2[O:29][CH:30]=[CH:31][C:17]=12>>[NH2:15][C:16]1[N:21]([C:22]2[CH:23]=[CH:24][C:25]([NH:28][C:12]([C:9]3([C:3]4[CH:4]=[C:5]([F:8])[CH:6]=[CH:7][C:2]=4[F:1])[CH2:11][CH2:10]3)=[O:13])=[CH:26][CH:27]=2)[CH2:20][N:19]=[C:18]2[O:29][CH:30]=[CH:31][C:17]=12참가 물질
3
실험 절차
The compound was prepared following the procedure described in Example 474, using 1-(2,5-Difluoro-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 407 [M+H]+.
후처리
- customThe compound was prepared
출처 및 근거
- ORD 기록
- ord-a2a5cdbcff964687b2196f46bfc49a30
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07427623B2
연결된 노트
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