Reaktionsgleichung
[N:1]1[CH:6]=[C:5]([C:7]([OH:9])=O)[CH:4]=[N:3][CH:2]=1.[CH:10]1([CH2:13][N:14]2[C:22]3[N:21]=[C:20]([CH2:23][C:24]4[CH:29]=[CH:28][C:27]([NH:30][CH3:31])=[CH:26][CH:25]=4)[NH:19][C:18]=3[C:17](=[O:32])[N:16]([CH2:33][C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=3[F:40])[C:15]2=[O:41])[CH2:12][CH2:11]1>CN(C)C1C=CN=CC=1>[CH:10]1([CH2:13][N:14]2[C:22]3[N:21]=[C:20]([CH2:23][C:24]4[CH:25]=[CH:26][C:27]([N:30]([CH3:31])[C:7]([C:5]5[CH:4]=[N:3][CH:2]=[N:1][CH:6]=5)=[O:9])=[CH:28][CH:29]=4)[NH:19][C:18]=3[C:17](=[O:32])[N:16]([CH2:33][C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=3[F:40])[C:15]2=[O:41])[CH2:12][CH2:11]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This compound was prepared by a method similar to that described in example 79 except that pyrimidine-5-carboxylic acid was used in place of N-acetyl-6-amino-2-pyridine carboxylic acid, the reaction was performed using 0.75 equivalents of 3-cyclopropylmethyl-8-[4-(methylamino)-benzyl]-1-(2-fluorobenzyl)-3,7-dihydropurine-2,6-dione and 1.5 equivalent of 4-dimethylaminopyridine was added as the final reagent to the reaction mixture. Purification was performed by chromatography using silica eluted with 94:6 ethyl acetate/methanol followed by trituration with hot acetonitrile to give the product as a colorless solid (72%). MS, m/z(M+H)=540.2161.
Aufarbeitung
- customThis compound was prepared by a method similar to
- customPurification
- washeluted with 94:6 ethyl acetate/methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-960f7c3a7ff645c88818ed6d406b2f06
- Quelldatensatz
- uspto-grants-2006_11
- Patentnummer
- US07135475B2
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