Reaktionsgleichung
[OH:1][C:2]1[C:7]([NH:8][C:9]2[C:10]3[C:17]([CH3:18])=[C:16]([C:19]([O:21][CH3:22])=[O:20])[S:15][C:11]=3[N:12]=[CH:13][N:14]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.O[CH:24]([CH3:34])[CH2:25][NH:26][C:27](=[O:33])[O:28][C:29]([CH3:32])([CH3:31])[CH3:30]>>[C:29]([O:28][C:27]([NH:26][CH2:25][CH:24]([O:1][C:2]1[C:7]([NH:8][C:9]2[C:10]3[C:17]([CH3:18])=[C:16]([C:19]([O:21][CH3:22])=[O:20])[S:15][C:11]=3[N:12]=[CH:13][N:14]=2)=[CH:6][CH:5]=[CH:4][N:3]=1)[CH3:34])=[O:33])([CH3:32])([CH3:31])[CH3:30]Komponenten
3
Versuchsvorschrift
Prepared analogously to example 9.1 using methyl 4-(2-hydroxypyridin-3-ylamino)-5-methylthieno[2,3-d]pyrimidine-6-carboxylate and tert-butyl N-(2-hydroxypropyl)-carbamate.
Quellen und Nachweise
- ORD-Eintrag
- ord-23c00a8f4fea4031b36c185393bbfb6d
- Quelldatensatz
- uspto-grants-2014_10
- Patentnummer
- US08853193B2
Verknüpfte Notizen
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