Basic information Safety Supplier Related

5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE

Basic information Safety Supplier Related

5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE Basic information

Product Name:
5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE
Synonyms:
  • 5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE
  • Methyl 4-(5-bromopyrimidin-2-yloxy)benzoate
  • 4-(5-Bromo-pyrimidin-2-yloxy)-benzoic acid methyl ester
  • 4-[(5-bromo-2-pyrimidinyl)oxy]Benzoic acid methyl ester
  • Methyl 4-((5-bromopyrimidin-2-yl)
  • Benzoic acid, 4-[(5-bromo-2-pyrimidinyl)oxy]-, methyl ester
  • 5-bromo-2-[(4-methoxycarbonyl)phenoxy]pyrimidine, CAS 926304-76-9
CAS:
926304-76-9
MF:
C12H9BrN2O3
MW:
309.12
Mol File:
926304-76-9.mol
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5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
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5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE Usage And Synthesis

Synthesis

32779-36-5

99-76-3

926304-76-9

Methyl 4-hydroxybenzoate (260 mg, 1.71 mmol) was dissolved in N,N-dimethylformamide (DMF, 25 mL) at room temperature, followed by the addition of 60% sodium hydride (NaH, 75 mg, 1.9 mmol). The reaction mixture was stirred for 30 min. After that, 5-bromo-2-chloropyrimidine (300 mg, 1.55 mmol) was added and the reaction system was heated to 130 °C and the reaction was maintained for 0.5 hours. After standard post-treatment and purification steps, the target product methyl 4-(5-bromopyrimidin-2-yloxy)benzoate (428 mg, 89% yield) was obtained.

References

[1] Patent: WO2007/22371, 2007, A2. Location in patent: Page/Page column 65

5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINESupplier

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