Reacción #3195

ord-1df0841ea5aa4fe28c1d99da441ccf1a

Ecuación de reacción

COC(=O)c1nc2ccccc2c(O)c1C(=O)OC
dimethyl 4-hydroxyquinoline-2,3-dicarboxylate
NN.O
hydrazine hydrate
O=c1[nH][nH]c(=O)c2c(O)c3ccccc3nc12
hydrazine
Rendimiento 112.8%
O=c1[nH][nH]c(=O)c2c(O)c3ccccc3nc12
2,3-Dihydro-10-hydroxypyridazino[4,5-b]quinoline-1,4-dione
Rendimiento 112.8%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISSOLUTIONdissolved
  2. 2
    TemperaturaThe resulting solution was refluxed for 3 hr during which time a thick precipitate
  3. 3
    Otroformed
  4. 4
    OtroThe cooled reaction mixture
  5. 5
    Filtraciónwas filtered
  6. 6
    Lavadothe collected yellow solids were washed with ethanol
  7. 7
    OtroAir drying

Procedimiento

To a stirred suspension of dimethyl 4-hydroxyquinoline-2,3-dicarboxylate (1.00 g, 3.83 mM, prepared as described by H. Biere and W. Seelen, Liebigs Ann. Chem. 1976, 1972) in ethanol (15 mL) was added hydrazine hydrate (9.64 g, 193 mM) whereupon the solids dissolved. The resulting solution was refluxed for 3 hr during which time a thick precipitate formed. The cooled reaction mixture was filtered and the collected yellow solids were washed with ethanol and then ether. Air drying provided 0.99 g of the hydrazine salt of 2,3-dihydro-10-hydroxypyridazino[4,5-b]quinoline-1,4-dione. This material was boiled in glacial acetic acid (40 mL) and, after cooling to room temperature, the mixture was filtered. The collected solids were washed with several portions of ethyl acetate and then ether. Air drying provided the title pyridazinodione (0.72 g, 82%) as a yellow solid, mp>400° C.; Mass Spectrum (Chemical Ionization): 230 (M+H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05733910uspto-grants-1998_03