HCID 69486807, Verbindung → HCID 22317960, Verbindung
Reaktionsgleichung
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([CH3:14])[C:11]([Cl:15])=[CH:10][C:9]=1[NH2:16])(C)(C)C.C(O[C:23](=[O:41])[CH2:24][C:25]([C:27]1[CH:32]=[CH:31][CH:30]=[C:29]([C:33]2[CH:38]=[C:37]([NH:39][CH3:40])[N:36]=[CH:35][N:34]=2)[CH:28]=1)=O)(C)(C)C>>[Cl:15][C:11]1[C:12]([CH3:14])=[CH:13][C:8]2[N:7]=[C:25]([C:27]3[CH:32]=[CH:31][CH:30]=[C:29]([C:33]4[CH:38]=[C:37]([NH:39][CH3:40])[N:36]=[CH:35][N:34]=4)[CH:28]=3)[CH2:24][C:23](=[O:41])[NH:16][C:9]=2[CH:10]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from (2-amino-4-chloro-5-methyl-phenyl)-carbamic acid tert-butyl ester (Example J22) (128 mg, 0.5 mmol) and 3-[3-(6-methylamino-pyrimidin-4-yl)-phenyl]-3-oxo-propionic acid tert-butyl ester (Example K54) (180 mg, 0.55 mmol) according to the general procedure M and subsequent treatment of the crude product according to the general procedure N. Obtained as a light yellow solid (132 mg).
Quellen und Nachweise
- ORD-Eintrag
- ord-9c7f0adec4ac410dbaba61a4e91b964b
- Quelldatensatz
- uspto-grants-2005_09
- DOI