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

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Products Intro: Product Name:2-Chloro-3-methylisonicotinic acid
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2-Chloro-3-Methyl-4-pyridinecarboxylic Acid manufacturers

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
EINECS:
Product Categories:
Mol File:133928-73-1.mol
2-Chloro-3-Methyl-4-pyridinecarboxylic Acid Structure
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
pka2.42±0.25(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C7H6ClNO2/c1-4-5(7(10)11)2-3-9-6(4)8/h2-3H,1H3,(H,10,11)
InChIKeyJYVLCHBMNCMRBO-UHFFFAOYSA-N
SMILESC1(Cl)=NC=CC(C(O)=O)=C1C
Safety Information
HS Code 2933399990
MSDS Information
2-Chloro-3-Methyl-4-pyridinecarboxylic Acid Usage And Synthesis
Uses2-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
2-Chloro-3-methyl-N-methyl-N-phenylisonicotinamide

133928-64-0

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

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
2-Chloro-3-Methyl-4-pyridinecarboxylic Acid Preparation Products And Raw materials
Raw materials2-Chloro-3-methyl-N-methyl-N-phenylisonicotinamide-->Sulfuric acid-->Hydrochloric acid-->Sodium carbonate
Tag:2-Chloro-3-Methyl-4-pyridinecarboxylic Acid(133928-73-1) Related Product Information
Benzoic acid 2-chloro-3-Methylisonicotinic acid 3-Amino-2-chloropyridine-4-carboxylic acid 2-CHLORO-3-METHYLPYRIDINE-4-CARBOXYLIC ACID ETHYL ESTER 2-Chloro-3-Methylisonicotinonitrile