7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one Basic information
- Product Name:
- 7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
- Synonyms:
-
- 7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
- 3-Oxo-3,4-dihydro-2H-1-oxa-4,5-diaza-7-broMo-naphthalene
- 7-Bromo-4H-pyrido[3,2-b][1,4]oxazin-3-one
- 7-BROMO-2H,4H-PYRIDO[3,2-B][1,4]OXAZIN-3-ONE
- 2H-Pyrido[3,2-b]-1,4-oxazin-3(4H)-one, 7-bromo-
- 7-bromo-2H,3H,4H-pyrido[3,2-b][1,4]oxazin-3-one
- CAS:
- 122450-96-8
- MF:
- C7H5BrN2O2
- MW:
- 229.03
- Mol File:
- 122450-96-8.mol
7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one Chemical Properties
- Boiling point:
- 403.9±45.0 °C(Predicted)
- Density
- 1.772
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 9.98±0.20(Predicted)
- Appearance
- White to off-white Solid
7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one Usage And Synthesis
Synthesis
20348-09-8
122450-96-8
General procedure for the synthesis of 7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-ones from 2H-pyrido[3,2-b][1,4]oxazin-3(4H)-ones: to 2H-pyrido[3,2-b][1,4]oxazin-3(4H)-ones (1 g, 6.66 mmol) of N,N-dimethylformamide (DMF. 30 mL) solution was slowly added bromine (0.480 mL, 9.32 mmol) dropwise. The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, deionized water was added to induce precipitate formation and the precipitate was collected by filtration. The resulting solid was dried overnight in a freeze dryer to afford 7-bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one (1.16 g, 76% yield). The product was characterized by 1H NMR (DMSO-d6): δ 11.43 (s, 1H), 8.04 (d, J = 2.0 Hz, 1H), 7.65 (d, J = 2.0 Hz, 1H), 4.67 (s, 2H).
References
[1] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 2, p. 133 - 142
[2] Patent: WO2009/100536, 2009, A1. Location in patent: Page/Page column 93-94
[3] Patent: WO2006/113432, 2006, A2. Location in patent: Page/Page column 56-57
[4] Patent: US4906629, 1990, A
[5] Patent: US4822794, 1989, A
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