Reaktion #72871

ord-4469cbe0f5874bb0a1dfebaf757e02f6

Reaktionsgleichung

Cl.N=C(N)N
guanidine hydrochloride
CCOC(=O)c1nn(C)c2c1CCC(=CN(C)C)C2=O
ethyl-6-[(dimethylamino)methylene]-1-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indazole-3-carboxylate
CCOC(=O)c1nn(C)c2c1ccc1cnc(N)nc12
Ethyl 8-amino-1-methyl-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate
Ausbeute 85.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 12 hours
  2. 2
    SonstigeThe solvent was then evaporated
  3. 3
    workup.DISSOLUTIONthe residue redissolved with dichloromethane
  4. 4
    Waschenwashed with water
  5. 5
    TrocknenThe organic layer was then dried over anhydrous Na2SO4
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe residue was triturated with diethyl ether
  8. 8
    Filtrationthe product collected by filtration (85% yield as a white solid)

Vorschrift

16.00 g (0.06 mol) of ethyl-6-[(dimethylamino)methylene]-1-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indazole-3-carboxylate were dissolved in 600 mL of ethanol and 3.90 g of sodium ethylate, and 5.44 g of guanidine hydrochloride were added consecutively. The solution was stirred at reflux for 12 hours. The solvent was then evaporated, the residue redissolved with dichloromethane and washed with water. The organic layer was then dried over anhydrous Na2SO4 and concentrated. The residue was triturated with diethyl ether and the product collected by filtration (85% yield as a white solid).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541429B2uspto-grants-2013_09