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Chemical Structure| 7033-50-3 Chemical Structure| 7033-50-3

Structure of 7033-50-3

Chemical Structure| 7033-50-3

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Product Details of [ 7033-50-3 ]

CAS No. :7033-50-3
Formula : C9H6ClNO2
M.W : 195.60
SMILES Code : O=C1OC(C)=NC2=CC=C(Cl)C=C12
MDL No. :MFCD00460088

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Application In Synthesis of [ 7033-50-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 7033-50-3 ]

[ 7033-50-3 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 7033-50-3 ]
  • [ 7142-09-8 ]
YieldReaction ConditionsOperation in experiment
82.7% at 130℃; for 7 h; General procedure: A solution of corresponding 2-methyl-4H-benzo[d][1,3]oxazin-4-one (16a-b) (1 mmol) in formamide (15 mL) was heated to 130 °C for 7 h (monitored by TLC & LCMS for completion). Upon cooling, the mixture got solidified, which was further washed with water, and recrystallized from ethanol to give 2-methylquinazolin-4(3H)-one (17a-b).
77% at 20℃; 6-chloro-2-methylquinazolin-4(3H)-one 10 g (58 mmol) 2-amino-5-chlorobenzoic acid was solved in 35 ml acetic anhydride and was stirred at reflux temperature for 4 hours. The reaction mixture was cooled down to room temperature and the solvent was rotary evaporated. The crude product was washed with hexane/ether 2:1 and than filtered. The solid 6-chloro-2-methyl-4H-3,1-benzoxazin-4-one (58 mmol) was suspended in 80 ml concentrated ammonium hydroxide and stirred at room temperature overnight. 10 percent sodium hydoxide solution was given to the reaction mixture resulting a transparent solution. The pH was adjusted to 7 with acetic acid. The product, which was precipitated from the solution, was filtered, washed with water and dried under vacuum overnight. Preparation of other 2-methylquinazolin-4(3H)-one derivatives were carried out with the same method. Yield: 8.76 g (77 percent) 1H NMR (300 MHz, DMSO-d6) δ ppm 7.98 (s, 1H); 7,76 (6Hz, d, 1H); 7.57 (9 Hz, d, 1H); 2.34 (s, 3H). LC-MS (ESI): m z (M+H)+ 195, Rt: 2.43 min.
References: [1] Farmaco, 1999, vol. 54, # 11-12, p. 780 - 784.
[2] European Journal of Medicinal Chemistry, 2014, vol. 86, p. 613 - 627.
[3] Patent: WO2015/19121, 2015, A1, . Location in patent: Page/Page column 8.
[4] Journal of Medicinal Chemistry, 1990, vol. 33, # 6, p. 1721 - 1728.
 

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