Potassium Iodide → methyl 7-methoxy-5-oxo-5H-thiazolo[2,3-b]quinazoline-2-carboxylate

HRID 1863238Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1863238
[CH3:1][O:2][C:3]1[CH:11]=[C:7]([C:8]([OH:10])=O)[C:6]([NH2:12])=[CH:5][CH:4]=1.Cl[C:14]1[S:15][C:16]([C:19]([O:21][CH3:22])=[O:20])=[CH:17][N:18]=1.[I-].[K+].C(=O)(O)[O-].[Na+]>>[CH3:1][O:2][C:3]1[CH:11]=[C:7]2[C:6](=[CH:5][CH:4]=1)[N:12]=[C:14]1[S:15][C:16]([C:19]([O:21][CH3:22])=[O:20])=[CH:17][N:18]1[C:8]2=[O:10]

Komponenten

5

Edukt 4

HCID 4875Potassium IodideHCID 2779305-Methoxyanthranilic acidHCID 516892Sodium BicarbonateHCID 12897294Methyl 2-chloro-1,3-thiazole-5-carboxylate

Produkt 1

HCID 15569301methyl 7-methoxy-5-oxo-5H-thiazolo[2,3-b]quinazoline-2-carboxylateAusbeute 33,3 %

Versuchsvorschrift

An intimate mixture of 1.49 g of 5-methoxyanthranilic acid, 1.58 g of methyl 2-chlorothiazole-5-carboxylate and 0.075 g of powdered potassium iodide was stirred and heated in an oil bath at 160°-165° for 80 minutes. The resultant dark solid was treated with 75 ml of a saturated solution of sodium bicarbonate and extracted with three portions of chloroform. The combined, dried (over magnesium sulfate) extract was concentrated in vacuo to a tan solid (1.59 g). Crystallization from methylene chloride-ether gave 0.86 g of methyl 7-methoxy-5-oxo-5H-thiazolo[2,3-b]quinazoline-2-carboxylate, having a melting point of 186°-192° C. This methyl ester was hydrolyzed by stirring for 16 hours at room temperature with 30 ml of 1 N sodium hydroxide and 30 ml of methanol. After filtration, the filtrate was acidified with acetic acid to pH5 and concentrated in vacuo. Water was added and the solid was removed by filtration. Since the base treatment also opens the lactam, this solid was refluxed for 1 hour in 75 ml of acetic acid. After concentration to 25 ml, the product crystallized on cooling and was filtered to give 0.53 of pure 7-methoxy-5-oxo-5H-thiazolo[2,3-b]quinazoline-2-carboxylic acid having a melting point of 247°-247.5° C.

Aufarbeitung

  1. temperatureheated in an oil bath at 160°-165° for 80 minutes
  2. extractionextracted with three portions of chloroform
  3. dry with materialdried (over magnesium sulfate)
  4. extractionextract
  5. concentrationwas concentrated in vacuo to a tan solid (1.59 g)
  6. customCrystallization from methylene chloride-ether

Quellen und Nachweise

ORD-Eintrag
ord-f7c4cd9bc061491cb039c6e6dd7f3dcc
Quelldatensatz
uspto-grants-1979_09
Patentnummer
US04168380

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