Basic information Safety Supplier Related

2-Chloro-3-Methyl-4-pyridinecarboxylic Acid

Basic information Safety Supplier Related

2-Chloro-3-Methyl-4-pyridinecarboxylic Acid Basic information

Product Name:
2-Chloro-3-Methyl-4-pyridinecarboxylic Acid
Synonyms:
  • 2-Chloro-3-Methyl-4-pyridinecarboxylic Acid
  • 2-chloro-3-Methylpyridine-4-carboxylic acid
  • 3-Methyl-2-chloro-4-pyridinecarboxylic acid
  • 3-Methyl-2-chloroisonicotinic acid
  • 3-Methyl-2-chloropyridine-4-carboxylic acid
  • 4-Pyridinecarboxylic acid, 2-chloro-3-methyl-
CAS:
133928-73-1
MF:
C7H6ClNO2
MW:
171.58
Mol File:
133928-73-1.mol
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2-Chloro-3-Methyl-4-pyridinecarboxylic Acid Chemical Properties

Boiling point:
412.7±40.0 °C(Predicted)
Density 
1.390±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
2.42±0.25(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C7H6ClNO2/c1-4-5(7(10)11)2-3-9-6(4)8/h2-3H,1H3,(H,10,11)
InChIKey
JYVLCHBMNCMRBO-UHFFFAOYSA-N
SMILES
C1(Cl)=NC=CC(C(O)=O)=C1C
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Safety Information

HS Code 
2933399990
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2-Chloro-3-Methyl-4-pyridinecarboxylic Acid Usage And Synthesis

Uses

2-Chloro-3-methylisonicotinic Acid is a derivative of Isonicotinic Acid (I821760) and is used as a reagent in the synthesis of N-pyridinylmethyl benzamide derivatives as anticancer agents.

Synthesis

133928-64-0

133928-73-1

Step 3: Synthesis of 2-chloro-3-methylpyridine-4-carboxylic acid A mixture of 2-chloro-N,3-dimethyl-N-phenylpyridine-4-carboxamide (2.2 g, 8.5 mmol) was mixed with a mixture of concentrated H2SO4 (23.2 mL) and water (16.8 mL), which was subsequently heated to 130 °C and kept for 46 hours. Upon completion of the reaction, the reaction mixture was cooled to room temperature and poured into ice (200 mL) and stirred until the ice was completely melted. The mixture was adjusted to alkaline (pH 8) by batchwise addition of solid Na2CO3 (50.3 g). The suspension was filtered and the filtrate was acidified to pH 3 by the addition of 6 M HCl (aq) (ca. 1.5 mL).The resulting solid was collected by filtration, washed with water (20 mL) and dried under vacuum at 40 °C for 10 h to afford 2-chloro-3-methyl-4-pyridinecarboxylic acid (779 mg, 54%) as a pink solid.LC-MS purity 100%, m/z = 171.9, 173.9; 1H NMR (500 MHz, MeOD) δ ppm 8.30 (d, J = 4.89 Hz, 1H), 7.64 (d, J = 5.04 Hz, 1H), 2.58 (s, 3H).

References

[1] Tetrahedron, 1991, vol. 47, # 9, p. 1697 - 1706
[2] Patent: WO2012/142513, 2012, A1. Location in patent: Page/Page column 427-428

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