5-(3-fluorophenyl)-10-hydroxy-1,3-dimethyl-7,8,9,10-tetrahydropyrimido[4,5-a]indolizine-2,4(1H,3H)-dione → 5-(3-Fluorophenyl)-10-hydroxy-1,3,8-trimethyl-7,8,9,10-tetrahydropyrimido[4,5-a]indolizine-2,4(1H,3H)-dione
반응식
FC1C=C(C2N3C(C(O)CCC3)=C3N(C)C(=O)N(C)C(=O)C=23)C=CC=1.FC1C=C(C2N3C(C(=O)CCC3)=C3N(C)C(=O)N(C)C(=O)C=23)C=CC=1.[F:51][C:52]1[CH:53]=[C:54]([C:58]2[N:66]3[C:61]([C:62](=[O:68])[CH2:63][CH:64]([CH3:67])[CH2:65]3)=[C:60]3[N:69]([CH3:76])[C:70](=[O:75])[N:71]([CH3:74])[C:72](=[O:73])[C:59]=23)[CH:55]=[CH:56][CH:57]=1>>[F:51][C:52]1[CH:53]=[C:54]([C:58]2[N:66]3[C:61]([CH:62]([OH:68])[CH2:63][CH:64]([CH3:67])[CH2:65]3)=[C:60]3[N:69]([CH3:76])[C:70](=[O:75])[N:71]([CH3:74])[C:72](=[O:73])[C:59]=23)[CH:55]=[CH:56][CH:57]=1참가 물질
4
반응물 3
생성물 1
실험 절차
The title compound was prepared analogously to Intermediate L using by replacing 5-(3-fluorophenyl)-1,3-dimethyl-8,9-dihydropyrimido[4,5-a]indolizine-2,4,10(1H,3H,7H)-trione in (step 2) with 5-(3-fluorophenyl)-1,3,8-trimethyl-8,9-dihydropyrimido[4,5-a]indolizine-2,4,10(1H,3H,7H)-trione.
출처 및 근거
- ORD 기록
- ord-5eea17f0aede40a88181a0f96c5a3d3e
- 출처 데이터셋
- uspto-grants-2016_06
- 특허 번호
- US09359381B2
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