ChemicalBook--->CAS DataBase List--->188781-10-4

188781-10-4

188781-10-4 Structure

188781-10-4 Structure
IdentificationBack Directory
[Name]

4-methyl-2-chloro-pyrimidine-5-carboxylic acid
[CAS]

188781-10-4
[Synonyms]

5-Carboxy-2-chloro-4-methylpyrimidine
4-ethyl-2-hydroxy-pyrimidine-5-carboxylic acid
2-chloro-4-methyl-5-Pyrimidine carboxylic acid
4-methyl-2-chloro-pyrimidine-5-carboxylic acid
5-Pyrimidinecarboxylic acid, 2-chloro-4-methyl-
5-Pyrimidinecarboxylic acid, 2-chloro-4-methyl- (9CI)
5-Carboxy-2-chloro-4-methylpyrimidine, 2-Chloro-4-methyl-1,3-diazine-5-carboxylic acid
[Molecular Formula]

C6H5ClN2O2
[MDL Number]

MFCD09863167
[MOL File]

188781-10-4.mol
[Molecular Weight]

172.57
Chemical PropertiesBack Directory
[Boiling point ]

375.3±22.0 °C(Predicted)
[density ]

1.479±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

powder
[pka]

2.06±0.25(Predicted)
[color ]

Faint yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

4-methyl-2-chloro-pyrimidine-5-carboxylic acid(188781-10-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE

188781-08-0

4-methyl-2-chloro-pyrimidine-5-carboxylic acid

188781-10-4

The general procedure for the synthesis of 2-chloro-4-methylpyrimidine-5-carboxylic acid from ethyl 4-methyl-2-chloropyrimidine-5-carboxylate is as follows: Example 9: Ethyl 2-chloro-4-methylpyrimidine-5-carboxylate (1.0 g, 5 mmol) was reacted with an aqueous solution (30 mL) of NaOH (0.24 g, 6 mmol) with stirring at room temperature for 3 hours. After completion of the reaction, the reaction solution was acidified with 6N HCl and the precipitated solid was filtered and dried to afford 2-chloro-4-methylpyrimidine-5-carboxylic acid (0.67 g, 78% yield). The product was characterized by 1H NMR (DMSO-d6): δ 9.01 (s, 1H), 2.75 (s, 3H).

[References]

[1] Journal of medicinal chemistry, 2000, vol. 43, # 21, p. 3995 - 4004
[2] Patent: US5935966, 1999, A
[3] Patent: US5811428, 1998, A
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