| Identification | Back Directory | [Name]
7-METHYLQUINAZOLIN-4(1H)-ONE | [CAS]
75844-40-5 | [Synonyms]
7-METHYLQUINAZOLIN-4(1H)-ONE 7-methylquinazolin-4(3H)-one 7-Methyl-4(3H)-quinazolinone 7-METHYL-1H-QUINAZOLIN-4-ONE 4(3H)-Quinazolinone, 7-methyl- 4(3H)-Quinazolinone, 7-methyl- >97% | [Molecular Formula]
C9H8N2O | [MDL Number]
MFCD10699397 | [MOL File]
75844-40-5.mol | [Molecular Weight]
160.17 |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 7-methyl-4(3H)-quinazolinone from 2-amino-4-methylbenzamide (1, 4.0 mmol) and compound (CAS: 77287-34-4, 2, 6.0 mmol): a mixture of 2-amino-4-methylbenzamide (1), formamide (2), Yb(OTf)3 (0.20 mmol, 5.0 mol%) and a mixture of homotrimethylbenzene (5.0 mL) were placed in a 20 mL Pyrex flask, the unit was equipped with a magnetic stir bar and a reflux condenser, and the reaction was carried out under argon protection. The reaction mixture was stirred at 120-165 °C (oil bath temperature) for 6 hours. After completion of the reaction, the mixture was cooled to room temperature and analyzed by GLC, GC-MS (EI) and LC-MS (ESI). After removal of homotrimethylbenzene by evaporation under vacuum, the product (3) was purified by recrystallization from methanol/hexane and/or silica gel medium pressure column chromatography (eluent: ethyl acetate/hexane = 50/50 to 100% ethyl acetate. For 3j, eluent: methanol/chloroform = 50/50). The structures of the products were confirmed by 1H NMR (400 MHz) and 13C NMR (100 MHz, DMSO-d6). The analytical and spectral data of compounds 3a-e, 3f, 3g, 3h and 3j were in agreement with literature reports. The product 3i was characterized as follows. | [References]
[1] Heterocycles, 2015, vol. 90, # 2, p. 857 - 865 |
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