1,2-Dichloroethane → HCID 178513561, Verbindung
Reaktionsgleichung
Br[C:2]1[C:7](Cl)=[CH:6][N:5]=[C:4]2[NH:9][CH:10]=[CH:11][C:3]=12.C(Cl)CCl.[CH:16]1[CH:17]=C[C:19]2[N:24](O)N=[N:22][C:20]=2[CH:21]=1.CN(C=[O:30])C>>[N:9]1[CH:10]=[CH:11][C:3]2[C:4]=1[NH:5][CH:6]=[CH:7][C:2]=2[C:16]1[CH:21]=[C:20]([C:19]([NH2:24])=[O:30])[NH:22][CH:17]=1Komponenten
5
Versuchsvorschrift
To a vial with Compound D′ (0.1 mmol) in DMF (1 mL), EDC (2 equivalent, 0.2 mmol) and HOBt (0.5 equivalent, 0.05 mmol) were added and the reaction mixture was stirred at room temperature for half an hour, amine (1.2 equivalent, 0.12 mmol) was added and the reaction mixture was stirred at room temperature for 2-3 hour. Reverse phase HPLC was used to purify the final compound.
Aufarbeitung
- stirringthe reaction mixture was stirred at room temperature for 2-3 hour
- customto purify the final compound
Quellen und Nachweise
- ORD-Eintrag
- ord-f2310ed1b88740c2b2f637a35f217648
- Quelldatensatz
- uspto-grants-2014_12
- Patentnummer
- US08921376B2
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