Reaktionsgleichung
[CH:1]1([C:4]2[N:9]=[C:8]([C:10]([NH:12][C:13]3[CH:17]=[N:16][N:15]([CH3:18])[C:14]=3[C:19](O)=[O:20])=[O:11])[C:7]([NH:22][C:23]3[CH:24]=[N:25][CH:26]=[N:27][CH:28]=3)=[N:6][CH:5]=2)[CH2:3][CH2:2]1.Cl.Cl.[CH3:31][N:32]1[CH2:35][CH:34]([NH2:36])[CH2:33]1>>[CH3:18][N:15]1[C:14]([C:19](=[O:20])[NH:36][CH:34]2[CH2:35][N:32]([CH3:31])[CH2:33]2)=[C:13]([NH:12][C:10]([C:8]2[C:7]([NH:22][C:23]3[CH:24]=[N:25][CH:26]=[N:27][CH:28]=3)=[N:6][CH:5]=[C:4]([CH:1]3[CH2:3][CH2:2]3)[N:9]=2)=[O:11])[CH:17]=[N:16]1Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The product was obtained starting from 4-{[6-cyclopropyl-3-(pyrimidin-5-ylamino)-pyrazine-2-carbonyl]-amino}-2-methyl-2H-pyrazole-3-carboxylic acid (30 mg, 79 μmol; example 236, step 3) and 1-methylazetidin-3-amine dihydrochloride (16 mg, 100 μmol) according to the method described in example 64, step 6 after purification by preparative HPLC using an acetonitrile/water gradient as yellow solid (11 mg, 31%).
Aufarbeitung
- customThe product was obtained
- customafter purification by preparative HPLC
Quellen und Nachweise
- ORD-Eintrag
- ord-f25b7e9d85a746179717a0dc8869d675
- Quelldatensatz
- uspto-grants-2014_04
- Patentnummer
- US08703768B2
Verknüpfte Notizen
Wird geladen…