Reaktionsgleichung
[Br:1][C:2]1[C:3]([CH3:9])=[N:4][C:5](Cl)=[CH:6][CH:7]=1.[CH3:10][N:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:14]2[CH2:15][CH2:16][N:11]([CH3:10])[CH2:12][CH2:13]2)=[N:4][C:3]=1[CH3:9]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 3-bromo-6-chloro-2-methylpyridine (700 mg, 3.39 mmol) and 1-methylpiperazine (0.753 mL, 6.78 mmol) in DMF (4 mL) was heated in microwave reactor at 150° C. for 50 minutes. The mixture was subsequently purified via preparative HPLC, eluting with a gradient of 10-70% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA) to give the title compound.
Aufarbeitung
- customThe mixture was subsequently purified via preparative HPLC
- washeluting with a gradient of 10-70% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA)
Quellen und Nachweise
- ORD-Eintrag
- ord-06e1793c54df47aa974c0aa09112478d
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09434743B2
Verknüpfte Notizen
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