Reaktion #306283

Reaktionsgleichung

1-(6-chloropyridazin-3-yl)hydrazine

2-(quinolin-6-yl)acetic acid

HCl

→

6-((6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline

Lösungsmittel

Na2CO3

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwas heated in a microwave (Personal Chemistry) at 180° C. & 15 min
2. 2
   SonstigeThe mixture was quenched with a solution of NaOH (1.2 g, 5 mL) slowly until the suspension
3. 3
   FiltrationThe mixture was filtered
4. 4
   Waschenwashed with H2O (2×5 mL)
5. 5
   SonstigeA brown solid was obtained (2.2 g)
6. 6
   Temperaturheated at 50° C. for 30 min
7. 7
   TemperaturThe blue mixture was cooled to room temperature
8. 8
   Filtrationfiltered
9. 9
   WaschenThe black solid was washed with H2O
10. 10
    Sonstigeto give the product

Vorschrift

A mixture of 1-(6-chloropyridazin-3-yl)hydrazine (1.67 g, 12 mmol), 2-(quinolin-6-yl)acetic acid (1.65 g, 8.8 mmol), and HCl (2000 μl, 24 mmol) was heated in an oil bath at 110° C. for 20 min before it was heated in a microwave (Personal Chemistry) at 180° C. & 15 min. The mixture was quenched with a solution of NaOH (1.2 g, 5 mL) slowly until the suspension is neutral in pH. The mixture was filtered and washed with H2O (2×5 mL). A brown solid was obtained (2.2 g). The solid was treated with aqueous Na2CO3 (3 g, 20 mL, pH ˜11) and heated at 50° C. for 30 min. The blue mixture was cooled to room temperature, and filtered. The black solid was washed with H2O and lyophilized to give the product. LCMS: calc'd for C15H10ClN5: 295.1; found 296.1 (M+1).

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