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2-Chloropyrimidine-4-carboxylic acid

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2-Chloropyrimidine-4-carboxylic acid Basic information

Product Name:
2-Chloropyrimidine-4-carboxylic acid
Synonyms:
  • CHEMBRDG-BB 4010944
  • AKOS BBS-00002507
  • 2-Chloropyrimidine-4-carboxylic acid
  • 4-Pyrimidinecarboxylic acid, 2-chloro-
  • 4-Carboxy-2-chloropyrimidine
  • 2-Chloro-pyrimidin-4-carboxylic acid
  • 4-Carboxy-2-chloropyrimidine, 4-Carboxy-2-chloro-1,3-diazine
  • 2-Chloropyrimidine-4-CarboxylicAci
CAS:
149849-92-3
MF:
C5H3ClN2O2
MW:
158.54
Product Categories:
  • Building Blocks
  • Heterocycle-Pyrimidine series
  • pyrimidine
  • pharmacetical
Mol File:
149849-92-3.mol
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2-Chloropyrimidine-4-carboxylic acid Chemical Properties

Boiling point:
411.4±18.0 °C(Predicted)
Density 
1.579
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
2.44±0.10(Predicted)
color 
Yellow
InChI
InChI=1S/C5H3ClN2O2/c6-5-7-2-1-3(8-5)4(9)10/h1-2H,(H,9,10)
InChIKey
YMDSUQSBJRDYLI-UHFFFAOYSA-N
SMILES
C1(Cl)=NC=CC(C(O)=O)=N1
CAS DataBase Reference
149849-92-3(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
22-26-36/37/39
HazardClass 
IRRITANT
HS Code 
29335990
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2-Chloropyrimidine-4-carboxylic acid Usage And Synthesis

Chemical Properties

Yellow to light brown or brown solid

Uses

2-Chloropyrimidine-4-carboxylic acid is a pharmaceutical intermediate compound used in the preparation of oxazolopyrimidine ketoamides with high active antagonism against TRPA1. This class of drugs can be used in the treatment of pain, itching, inflammation, asthma, cough and other related conditions.

Synthesis

149849-93-4

149849-92-3

Example 5 Preparation of 2-chloropyrimidine-4-carboxamide: Ammonia was passed into 20 mL of tetrahydrofuran for 35 minutes at -6 °C. The reaction system was then warmed to 10 °C and 1.5 g (8.47 mmol) of 2-chloropyrimidine-4-carbonyl chloride was added. The reaction solution was stirred at room temperature for 45 min. Upon completion of the reaction, the reaction solution was concentrated using a rotary evaporator and the residue was poured into 90 mL of saturated NaHCO3 solution. The aqueous phase was extracted three times with 50 mL of ethyl acetate. The organic phases were combined, washed with saturated NaCl solution, dried over anhydrous Na2SO4 and concentrated again using a rotary evaporator. After drying under high vacuum, 1.07 g of white solid product was obtained in 80% yield (based on 2-chloropyrimidine-4-carbonyl chloride). The melting point of the product ranged from 147.2 °C to 151.4 °C. The product was characterized by the following data: 1H-NMR (CDCl3, 300 MHz) δ (ppm): 6.2 (br.s), 7.25 (s), 7.7 (br.s), 8.1 (d), 8.9 (d).

References

[1] Patent: US5591853, 1997, A

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