반응식
[NH2:1][C:2]1[CH:3]=[C:4]([NH:18][C:19](=[O:27])[C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)[CH:5]=[CH:6][C:7]=1[C:8]1[N:12]([CH3:13])[N:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=1.CCN(C(C)C)C(C)C.[C:37](Cl)(=[O:39])[CH3:38].C(Cl)Cl.C([O-])(O)=O.[Na+]>C(Cl)Cl.O>[C:37]([NH:1][C:2]1[CH:3]=[C:4]([NH:18][C:19](=[O:27])[C:20]2[CH:21]=[CH:22][C:23]([Cl:26])=[CH:24][CH:25]=2)[CH:5]=[CH:6][C:7]=1[C:8]1[N:12]([CH3:13])[N:11]=[C:10]([C:14]([F:17])([F:15])[F:16])[CH:9]=1)(=[O:39])[CH3:38]참가 물질
7
실험 절차
To a solution of 17 (20 mg) in 2 ml DCM was added 3 eq DIEA and acetyl chloride (20 μl). The reaction mixture was stirred at r.t. for 5 h before worked up with DCM/NaHCO3, water. The org. phase was concentrated and subjected to prep HPLC purification to furnish compound 18.
후처리
- concentrationphase was concentrated
- customHPLC purification
출처 및 근거
- ORD 기록
- ord-3de7907d9ec1449ea9857ca5a3100662
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08754219B2
연결된 노트
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