Basic information Safety Supplier Related

6-METHOXY-7-HYDROXYQUINAZOLIN-4-ONE

Basic information Safety Supplier Related

6-METHOXY-7-HYDROXYQUINAZOLIN-4-ONE Basic information

Product Name:
6-METHOXY-7-HYDROXYQUINAZOLIN-4-ONE
Synonyms:
  • 6-METHOXY-7-HYDROXYQUINAZOLIN-4-ONE
  • 7-Hydroxy-6-Methoxy-3,4-d...
  • 7-Hydroxy-6-Methoxy-3,4-dihydroquinazolin-4-one
  • 6-Methoxy-7-Hydroxyquinazoline-4-One
  • 6-methoxy-7-hydydroxyquinazoline-4-one
  • 7-hydroxy-6-methoxyquinazolin-4(1H)-one
  • 7-hydroxy-6-methoxy-4(3H)-Quinazolinone
  • 7-Hydroxy-6-methoxy-3H-quinazolin-4-one
CAS:
162012-72-8
MF:
C9H8N2O3
MW:
192.17
Mol File:
162012-72-8.mol
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6-METHOXY-7-HYDROXYQUINAZOLIN-4-ONE Chemical Properties

Melting point:
>255oC (dec.)
Boiling point:
420.0±55.0 °C(Predicted)
Density 
1.47±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly, Heated), Methanol (Slightly, Heated)
pka
8.07±0.20(Predicted)
form 
Solid
color 
Light Beige
InChI
InChI=1S/C9H8N2O3/c1-14-8-2-5-6(3-7(8)12)10-4-11-9(5)13/h2-4,12H,1H3,(H,10,11,13)
InChIKey
ZHLRYPLSYOYNQM-UHFFFAOYSA-N
SMILES
N1C2=C(C=C(OC)C(O)=C2)C(=O)NC=1
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Safety Information

HS Code 
2933998090
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6-METHOXY-7-HYDROXYQUINAZOLIN-4-ONE Usage And Synthesis

Uses

7-Hydroxy-6-methoxy-3,4-dihydroquinazolin-4-one is a potential 2-arylbenzothiazoles based kinase inhibitor.

Synthesis

179688-01-8

162012-72-8

General procedure for the synthesis of 6-methoxy-7-(benzyloxy)quinazolin-4(3H)-one from 6-methoxy-7-hydroxyquinazolin-4-one: Compound 122 (247 g, 875.6 mmol) was dissolved in trifluoroacetic acid (800 mL), followed by a one-time addition of methanesulfonic acid (127 mL). The reaction mixture was heated to reflux and maintained for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated. To the concentrated mixture, 2.5 N of aqueous sodium hydroxide was added and the pH of the solution was adjusted to 7, at which point precipitation was observed to be generated. The resulting solid was pulverized and subjected to vigorous stirring for 1 hour followed by filtration operation. The solid product was collected and dried under high vacuum to give the final compound 123 (148 g, yield = 88%) presenting as a brown solid.

References

[1] Tetrahedron Letters, 2005, vol. 46, # 43, p. 7381 - 7384
[2] Patent: US2014/235634, 2014, A1. Location in patent: Paragraph 0390; 0395
[3] Patent: WO2004/94410, 2004, A1. Location in patent: Page 122
[4] Patent: WO2004/113324, 2004, A1. Location in patent: Page 52
[5] Patent: WO2005/13998, 2005, A1. Location in patent: Page/Page column 60

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