Reaktionsgleichung
CC[C@@H]([C@H](NC([C@@H](NC([C@@H](NC([C@@H](N)C)=O)C)=O)CO)=O)C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H:56]([C:64](O)=O)[CH2:57][CH2:58][CH2:59][N:60]=[C:61]([NH2:63])N)=O)CC(O)=O)=O)C)=O)CO)=O)C(C)C)=O)C)=O)C(C)C)=O)CCCCN)=O)C.CC1C=[CH:89][N:88]=CN=1.[CH3:91][C:92]1[CH:93]=[C:94]([CH:99]=[CH:100][CH:101]=1)C(OC)=O.FC1C=CC(C(CC2C=C[N:113]=CC=2)=O)=CC=1>>[CH3:91][C:92]1[CH:93]=[C:94]([C:64]2[C:56]([C:57]3[CH:58]=[CH:59][N:60]=[CH:61][N:63]=3)=[CH:89][NH:88][N:113]=2)[CH:99]=[CH:100][CH:101]=1Komponenten
5
Versuchsvorschrift
This compound was prepared by the same procedure as described for Example A-208 except that 1-methyl-3-(4′-pyrimidinylacetyl)benzene (prepared as set forth in Step 1 of Example A-19 from 4-methyl-pyrimidine and methyl 3-methylbenzoate) was used in place of 4-fluorobenzoyl-4-pyridinyl methane.
Aufarbeitung
- customThis compound was prepared by the same procedure
- customprepared
Quellen und Nachweise
- ORD-Eintrag
- ord-115ebaf4e5d94608ab014f3be21bf72b
- Quelldatensatz
- uspto-grants-2005_12
- Patentnummer
- US06979686B1
Verknüpfte Notizen
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