Methanol → Methyl pyridazine-4-carboxylate

HRID 578149

Reaktionsgleichung

Reaktionsgleichung von HRID 578149
[N:1]1[CH:6]=[CH:5][C:4]([C:7]([OH:9])=[O:8])=[CH:3][N:2]=1.S(=O)(=O)(O)O.[CH3:15]O>>[N:1]1[CH:6]=[CH:5][C:4]([C:7]([O:9][CH3:15])=[O:8])=[CH:3][N:2]=1

Komponenten

4

Versuchsvorschrift

To a solution of pyridazine-4-carboxylic acid (Aldrich, 5.0 g, 40.3 mmol) in methanol (anhydrous, Aldrich, 100 mL) was added sulfuric acid (concentrated, Aldrich, 2 mL). The reaction mixture was then heated to reflux and stirred for 16 hours. The volatiles were removed under reduced pressure. The residue was basified to pH=8-9 with saturated sodium carbonate (20 mL) and then extracted with EtOAc (3×100 mL). The combined extracts were washed with brine (2×20 mL) and dried over magnesium sulfate. The drying agent was filtered off and the organic solution was concentrated and dried to give the titled compound. 1H NMR (300 MHz, DMSO-d6) δ 3.34 (s, 3H), 8.10 (dd, J=5.2, 2.4 Hz, 1H), 9.52 (dd, J=5.2, 1.2 Hz, 1H), 9.58 (dd, J=2.2, 1.4 Hz, 1H) ppm; MS (DCI/NH3) m/z 139 (M+H)+.

Aufarbeitung

  1. temperatureThe reaction mixture was then heated
  2. temperatureto reflux
  3. customThe volatiles were removed under reduced pressure
  4. extractionextracted with EtOAc (3×100 mL)
  5. washThe combined extracts were washed with brine (2×20 mL)
  6. dry with materialdried over magnesium sulfate
  7. filtrationThe drying agent was filtered off
  8. concentrationthe organic solution was concentrated
  9. customdried

Quellen und Nachweise

ORD-Eintrag
ord-a15ae1295bd14bc2b11d16b24482d131
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09040568B2

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