반응식
Br[C:2]1[CH:3]=[C:4]2[C@@:15]3([CH2:19][O:18][C:17]([NH2:20])=[N:16]3)[C:14]3[CH:13]=[C:12](Cl)[N:11]=[C:10]([F:22])[C:9]=3[O:8][C:5]2=[CH:6][CH:7]=1.[N:23]1[CH:28]=[CH:27][CH:26]=[C:25](B(O)O)[CH:24]=1.Cl.[F:33][C:34]1([F:39])[CH2:38][CH2:37][NH:36][CH2:35]1>>[F:33][C:34]1([F:39])[CH2:38][CH2:37][N:36]([C:12]2[N:11]=[C:10]([F:22])[C:9]3[O:8][C:5]4[C:4]([C@@:15]5([CH2:19][O:18][C:17]([NH2:20])=[N:16]5)[C:14]=3[CH:13]=2)=[CH:3][C:2]([C:25]2[CH:24]=[N:23][CH:28]=[CH:27][CH:26]=2)=[CH:7][CH:6]=4)[CH2:35]1참가 물질
4
반응물 3
생성물 1
실험 절차
The title compound was synthesized by steps analogous to those described in method CC4 above, but using (S)-7-bromo-3-chloro-1-fluoro-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine (prepared by steps analogous to those described in Method BB33) and 3-pyridyl-boronic acid and 3,3-difluoropyrrolidine hydrochloride.
후처리
- customprepared by steps analogous to
출처 및 근거
- ORD 기록
- ord-a85f3a430f2c437fb71eff867eaedbde
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08883782B2
연결된 노트
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