ChemicalBook--->CAS DataBase List--->926304-76-9

926304-76-9

926304-76-9 Structure

926304-76-9 Structure
IdentificationBack Directory
[Name]

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

926304-76-9
[Synonyms]

Methyl 4-((5-bromopyrimidin-2-yl)
Methyl 4-(5-bromopyrimidin-2-yloxy)benzoate
5-BROMO-2-[(4-METHOXYCARBONYL)PHENOXY]PYRIMIDINE
4-(5-Bromo-pyrimidin-2-yloxy)-benzoic acid methyl ester
4-[(5-bromo-2-pyrimidinyl)oxy]Benzoic acid methyl ester
Benzoic acid, 4-[(5-bromo-2-pyrimidinyl)oxy]-, methyl ester
[Molecular Formula]

C12H9BrN2O3
[MDL Number]

MFCD09743706
[MOL File]

926304-76-9.mol
[Molecular Weight]

309.12
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
Hazard InformationBack Directory
[Synthesis]

5-Bromo-2-chloropyrimidine

32779-36-5

Methylparaben

99-76-3

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

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
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