Sodium Hydroxide → 5-oxo-1H,5H-pyrazolo[1,5-a]quinazoline-3-carboxylic acid

HRID 1927289Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1927289
Cl.[NH:2]([C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6]([OH:8])=O)[NH2:3].[C:13](/[C:15](=[CH:21]\OCC)/[C:16]([O:18]CC)=[O:17])#[N:14].C([O-])(=O)C.[Na+].[OH-].[Na+]>CN(C=O)C.O>[O:8]=[C:6]1[C:5]2[C:4](=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:2]2[N:3]=[CH:21][C:15]([C:16]([OH:18])=[O:17])=[C:13]2[NH:14]1

Komponenten

7

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

A mixture of 2-hydrazinylbenzoic acid hydrochloride (1.05 g, 5.57 mmol), (E)-ethyl 2-cyano-3-ethoxyacrylate (0.9 g, 5.32 mmol) and sodium acetate (0.457 g, 5.57 mmol) in DMF (7 mL) was heated to 140° C. for 2 h then cooled. Water (5 mL) was added and the mixture was stirred at rt for 1 h then filtered. The solid was washed with H2O, EtOH and Et2O then dried. The solid was dissolved in EtOH (10 mL), treated with a 1M solution of sodium hydroxide (23 mL, 23 mmol) and the mixture was heated at 80° C. for 18 hr. The mixture was filtered hot then cooled and acidified with acetic acid and 10% HCl. The precipitated product was filtered, washed with H2O and Et2O, dried well and used without any further purification.

Aufarbeitung

  1. temperaturethen cooled
  2. filtrationthen filtered
  3. washThe solid was washed with H2O, EtOH and Et2O
  4. customthen dried
  5. dissolutionThe solid was dissolved in EtOH (10 mL)
  6. temperaturethe mixture was heated at 80° C. for 18 hr
  7. filtrationThe mixture was filtered hot
  8. temperaturethen cooled
  9. filtrationThe precipitated product was filtered
  10. washwashed with H2O and Et2O
  11. customdried well
  12. customused without any further purification

Quellen und Nachweise

ORD-Eintrag
ord-b70e400a1452480db80a12716f69c54d
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08183250B2

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