ChemicalBook--->CAS DataBase List--->16064-24-7

16064-24-7

16064-24-7 Structure

16064-24-7 Structure
IdentificationBack Directory
[Name]

7-METHOXY-4(1H)-QUINAZOLINONE
[CAS]

16064-24-7
[Synonyms]

7-METHOXY-4(1H)-QUINAZOLINONE
7-Methoxyquinazolin-4(1H)-one
7-Methoxy-4(3h)-quinazolinone
7-Methoxy-3H-quinazolin-4-one
7-Methoxyquinazolin-4(3H)-one
4(3H)-Quinazolinone, 7-methoxy-
7-methoxy-1,4-dihydroquinazolin-4-one
[Molecular Formula]

C9H8N2O2
[MDL Number]

MFCD08460971
[MOL File]

16064-24-7.mol
[Molecular Weight]

176.17
Chemical PropertiesBack Directory
[Melting point ]

257-258℃
[Boiling point ]

338.7±44.0 °C(Predicted)
[density ]

1.32
[storage temp. ]

2-8°C
[pka]

1.51±0.20(Predicted)
[Appearance]

Brown to black Solid
Safety DataBack Directory
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

7-METHOXY-4(1H)-QUINAZOLINONE(16064-24-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Formamidine acetate

3473-63-0

2-AMINO-4-METHOXY-BENZOIC ACID

4294-95-5

7-METHOXY-4(1H)-QUINAZOLINONE

16064-24-7

The general procedure for the synthesis of 7-methoxyquinazolin-4(1H)-one from formamidine acetate and 2-amino-4-methoxybenzoic acid was as follows: 1. 2-Amino-4-methoxybenzoic acid (4.85 g, 28.9 mmol) and formamidine acetate (18.49 g, 177.8 mmol) were mixed in 100 mL of 2-methoxyethanol. 2. The reaction mixture was heated to reflux and stirred under these conditions for 12 hours. 3. After completion of the reaction, the mixture was cooled to 25 °C. The reaction was carried out with 0.01 M 4. Dilute the cooled reaction mixture with 0.01 M aqueous ammonia solution (100 mL). 5. Continue stirring at 25 °C for 30 min. 6. Collect the light brown solid product formed by filtration. 7. Wash the solid product with 0.01 M aqueous ammonia solution. 8. 8. The final product 7-methoxyquinazolin-4(1H)-one was obtained by high vacuum drying in a yield of 11.5 g (73% yield). Product characterization data: NMR (δ, ppm): 12.10 (s, br, 1H), 8.05 (m, 2H), 7.10 (m, 2H), 3.90 (s, 3H); m/z 167.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 17, p. 4963 - 4966
[2] Patent: WO2007/71963, 2007, A2. Location in patent: Page/Page column 52
[3] Patent: CN104447769, 2016, B. Location in patent: Paragraph 0056-0057
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