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19181-54-5

19181-54-5 Structure

19181-54-5 Structure
IdentificationBack Directory
[Name]

8-METHYL-4-QUINAZOLONE
[CAS]

19181-54-5
[Synonyms]

8-METHYL-4-QUINAZOLONE
8-Methylquinazolin-4-ol
8-Methylquinazolin-4(3H)
8-methyl-4-quinazolinone
8-methylquinazolin-4(1H)-one
8-METHYL-3H-QUINAZOLIN-4-ONE
8-methyl-1H-quinazolin-4-one
8-Methylquinazolin-4(3H)-one
8-Methylquinazolin-4(3H)-one98%
8-Methylquinazolin-4(3H)-one 98%
8-Methyl-3,4-dihydroquinazolin-4-one
8-METHYL-4-QUINAZOLONE ISO 9001:2015 REACH
[Molecular Formula]

C9H8N2O
[MDL Number]

MFCD01685945
[MOL File]

19181-54-5.mol
[Molecular Weight]

160.17
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[color ]

Faint beige
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P261-P280
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2933998090
Hazard InformationBack Directory
[Synthesis Reference(s)]

Synthetic Communications, 14, p. 1013, 1984 DOI: 10.1080/00397918408059628
[Synthesis]

3-Methylanthranilic acid

4389-45-1

formamide

77287-34-4

8-METHYL-4-QUINAZOLONE

19181-54-5

Formamide (26 mL, 0.6600 mol) was added to 2-amino-3-methylbenzoic acid (100 g, 0.66 mol) and formamidine acetate (206 g, 1.98 mol) in a 2L round-bottomed flask equipped with a mechanical stirrer. The reaction mixture was heated at 160 °C for 16 h. The reaction process was monitored by LCMS. After completion of the reaction, the mixture was cooled to room temperature and diluted with 2N NaOH solution (300 mL). After stirring for 15 min at room temperature, the reaction mixture was neutralized with 1.5N HCl solution. The precipitated solid product was collected by filtration, washed with ice water and dried under vacuum to afford 8-methyl-4-quinazolone (90 g, 86% yield) as an off-white solid. The structure of the product was confirmed by 1H NMR (DMSO-d6, 400 MHz): δ 12.21 (bs, 1H), 8.10 (s, 1H), 7.95-7.93 (dd, J = 8.8, 7.9 Hz, 1H), 7.65-7.63 (d, J = 7.9 Hz, 1H), 7.39-7.35 (t, J = 15.2 Hz, 1H ), 2.51 (s, 3H).

[References]

[1] Patent: WO2013/96194, 2013, A1. Location in patent: Page/Page column 28-29
[2] European Journal of Medicinal Chemistry, 2012, vol. 50, p. 264 - 273
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 6, p. 2794 - 2809
[4] Chemische Berichte, 1905, vol. 38, p. 3555
[5] Journal of Organic Chemistry, 1952, vol. 17, p. 149,153
Spectrum DetailBack Directory
[Spectrum Detail]

8-METHYL-4-QUINAZOLONE(19181-54-5)1HNMR
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