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852180-74-6

852180-74-6 Structure

852180-74-6 Structure
IdentificationBack Directory
[Name]

3-PYRIMIDIN-5-YL-BENZOIC ACID
[CAS]

852180-74-6
[Synonyms]

P-017
AKOS BAR-0650
3-(2-Methoxyp
3-(5-PYRIMIDINYL)BENZOIC ACID
3-PYRIMIDIN-5-YL-BENZOIC ACID
3-PYRIMIDIN-5-YL-BENZOIC ACID, 95+%
Benzoic acid, 3-(5-pyrimidinyl)- (9CI)
3-(2-Chloropyrimidin-5-yl)benzoic acid
3-(2,4-Dimethoxypyrimidin-5-yl)benzoic acid
3-(2-(Methylthio)pyrimidin-5-yl)benzoic acid
3-(2-Oxo-1,2-dihydropyrimidin-5-yl)benzoic acid
3-PYRIMIDIN-5-YL-BENZOIC ACID ISO 9001:2015 REACH
3-(3-(Dimethylamino)-2-methoxypyrimidin-5-yl)benzoic acid
[Molecular Formula]

C11H8N2O2
[MDL Number]

MFCD05864810
[MOL File]

852180-74-6.mol
[Molecular Weight]

200.19
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder
[color ]

Off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

3-PYRIMIDIN-5-YL-BENZOIC ACID(852180-74-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Bromopyrimidine

4595-59-9

3-Carboxyphenylboronic acid pinacol ester

269409-73-6

3-PYRIMIDIN-5-YL-BENZOIC ACID

852180-74-6

General method: 5-Bromopyrimidine (1.0 eq.) was dissolved in a solvent mixture of water and dioxane (1:1). Subsequently 3-carboxyphenylboronic acid pinacol ester (1.5 eq.) and potassium phosphate (5.0 eq.) were added. The reaction solution was degassed by vacuum/argon cycle (10 times) and further degassed (5 times) before addition of PdCl2(PPh3)2 (10 mol%). The resulting mixture was stirred and reacted at 95 °C and under argon protection for 16-20 hours. Upon completion of the reaction, the mixture was filtered through diatomaceous earth and diluted with about 30 mL of water and subsequently washed with chloroform (3 x 30 mL). Unless otherwise indicated, the aqueous phase was concentrated under reduced pressure and purified by C18 pre-column and further eluted on a 10g or 60g C18 column using gradient elution with aqueous acetonitrile (10-100%) to obtain the target product 3-pyrimidine-5-benzene carboxylic acid.

[References]

[1] European Journal of Medicinal Chemistry, 2018, vol. 145, p. 634 - 648
[2] Patent: WO2016/34673, 2016, A1. Location in patent: Page/Page column 80
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