6-Amino-3-chloropyridazine → HCID 178484245, Verbindung

HRID 2176619

Reaktionsgleichung

Reaktionsgleichung von HRID 2176619
[Cl:1][C:2]1[N:7]=[N:6][C:5]([NH2:8])=[CH:4][CH:3]=1.CO[CH:11](OC)[N:12]([CH3:14])[CH3:13]>>[Cl:1][C:2]1[N:7]=[N:6][C:5](/[N:8]=[CH:11]/[N:12]([CH3:14])[CH3:13])=[CH:4][CH:3]=1

Komponenten

3

Edukt 2

HCID 216436-Amino-3-chloropyridazineHCID 78373Dimethylformamide dimethyl acetal

Produkt 1

HCID 178484245HCID 178484245, VerbindungAusbeute 82,9 %

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

A 500 mL RB flask was charged with 6-chloropyridazin-3-amine (10.0 g, 77.2 mmol) and dimethoxy-N,N-dimethylmethanamine (206 ml, 1544 mmol), equipped with a reflux condenser, then heated to 110° C. for 3 hours then left at room temperature for 16 hours. The precipitate was collected by filtration. The mother liquor was concentrated down to give an yellow solid, which was triturated with EtOAc and collected. The solids were combined to give (E)-N′-(6-chloropyridazin-3-yl)-N,N-dimethylformamidine (11.81 g, 82.9% yield) as a white solid

Aufarbeitung

  1. customequipped with a reflux condenser
  2. filtrationThe precipitate was collected by filtration
  3. concentrationThe mother liquor was concentrated down
  4. customto give an yellow solid, which
  5. customwas triturated with EtOAc
  6. customcollected

Quellen und Nachweise

ORD-Eintrag
ord-866037ccb2c548d89a4cadf36b178b9f
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09066954B2

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