반응식
FC1C=C(C2C3CN(C(OC(C)(C)C)=O)CCC=3[NH:11][N:10]=2)C=CC=1F.[O:25]1[CH2:30][CH2:29][CH2:28][C:27](=O)[CH2:26]1.[Cl:32][C:33]1[CH:34]=[CH:35][C:36]([F:42])=[C:37]([CH:41]=1)[C:38](Cl)=O>>[Cl:32][C:33]1[CH:34]=[CH:35][C:36]([F:42])=[C:37]([C:38]2[C:28]3[CH2:29][CH2:30][O:25][CH2:26][C:27]=3[NH:10][N:11]=2)[CH:41]=1참가 물질
4
실험 절차
Intermediate 16C was prepared according to the procedure for the synthesis of intermediate 15 by replacing 1-Boc-4-piperidone with dihydro-2H-pyran-3(4H)-one, and replacing 3,4-difluorobenzoyl chloride with 5-chloro-2-fluorobenzoyl chloride. LCMS (+ESI) m/z=253 [M+H]+.
출처 및 근거
- ORD 기록
- ord-dbdbeb6fa9e542b3be984fed265beae6
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07741350B1
연결된 노트
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