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methyl 6-methylpyridine-2-carboxylate

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Products Intro: Product Name:methyl 6-methylpyridine-2-carboxylate
CAS:13602-11-4
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Products Intro: Product Name:Methyl 6-methylpicolinate
CAS:13602-11-4
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:13602-11-4
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Products Intro: Product Name:Methyl 6-methylpyridine-2-carboxylate(13602-11-4)
CAS:13602-11-4
Purity:99% Package:25KG;5KG;1KG

methyl 6-methylpyridine-2-carboxylate manufacturers

methyl 6-methylpyridine-2-carboxylate Basic information
Product Name:methyl 6-methylpyridine-2-carboxylate
Synonyms:methyl 6-methylpyridine-2-carboxylate;2-Pyridinecarboxylicacid,6-methyl-,methylester(9CI);METHYL-6-MENTHYPYRIDINE-2-CARBOXYLATE;6-Methyl-2-pyridinecarboxylic acid methyl ester;Methyl 6-methyl-2-pyridinecarboxylate;Methyl 6-methylpicolinate;NSC 109151;2-Pyridinecarboxylic acid, 6-Methyl-, Methyl ester
CAS:13602-11-4
MF:C8H9NO2
MW:151.16
EINECS:237-085-0
Product Categories:Heterocycle-Pyridine series;CARBOXYLICESTER;GLYCINESCAFFOLD
Mol File:13602-11-4.mol
methyl 6-methylpyridine-2-carboxylate Structure
methyl 6-methylpyridine-2-carboxylate Chemical Properties
Melting point 18 °C
Boiling point 242℃
density 1.104
refractive index 1.5160-1.5200
Fp 100℃
storage temp. Inert atmosphere,Room Temperature
pka1.93±0.10(Predicted)
form powder to lump to clear liquid
color White or Colorless to Light yellow
Safety Information
HS Code 2933399990
MSDS Information
methyl 6-methylpyridine-2-carboxylate Usage And Synthesis
UsesMethyl 6-Methylpyridine-2-carboxylate is a reagent used in the sunthesis of antitumor agents based upon the dihydropyrrolopyrazole compounds. Also used in the synthesis of quinazolinone TGF-β inhibitors.
Synthesis
Methanol

67-56-1

6-Methyl-2-pyridinecarboxylic acid

934-60-1

methyl 6-methylpyridine-2-carboxylate

13602-11-4

Step 2: 26.8 g (0.195 mol) of SOCl2 was slowly added dropwise to 100 mL of methanol at a low temperature of -10 °C while stirring was continued. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature and stirring was continued for 1 hour. Subsequently, 10 g of 6-methyl-2-pyridinecarboxylic acid (Compound 2) was added to the reaction system and the reaction was refluxed at 80 °C for 5 hours. Upon completion of the reaction, 10.2 g of methyl 6-methyl-2-pyridinecarboxylate (Compound 3) was obtained in 93% yield.

References[1] Patent: CN105294552, 2016, A. Location in patent: Paragraph 0047; 0051
[2] Patent: WO2004/48383, 2004, A1. Location in patent: Page 40
[3] Patent: WO2004/48382, 2004, A1. Location in patent: Page 8
[4] Patent: WO2016/187308, 2016, A1. Location in patent: Paragraph 0349
[5] Patent: WO2012/80221, 2012, A1. Location in patent: Page/Page column 98
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