methyl 2,6-dichloro-4-methylnicotinate

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methyl 2,6-dichloro-4-methylnicotinate Basic information
Product Name:methyl 2,6-dichloro-4-methylnicotinate
Synonyms:methyl 2,6-dichloro-4-methylnicotinate;2,6-Dichloro-4-methylnicotinic acid methyl ester;2,6-Dichloro-4-methylpyridine-3-carboxylic acid methyl ester;3-Pyridinecarboxylic acid, 2,6-dichloro-4-methyl-, methyl ester;methyl 2,6-dichloro-4-methyl-pyridine-3-carboxylate
CAS:1013648-04-8
MF:C8H7Cl2NO2
MW:220.05
EINECS:
Product Categories:
Mol File:1013648-04-8.mol
methyl 2,6-dichloro-4-methylnicotinate Structure
methyl 2,6-dichloro-4-methylnicotinate Chemical Properties
Boiling point 292℃
density 1.369
Fp 130℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-3.75±0.10(Predicted)
AppearanceLight brown to yellow Solid
InChIInChI=1S/C8H7Cl2NO2/c1-4-3-5(9)11-7(10)6(4)8(12)13-2/h3H,1-2H3
InChIKeyQOTFUYQFPHLJTM-UHFFFAOYSA-N
SMILESC1(Cl)=NC(Cl)=CC(C)=C1C(OC)=O
Safety Information
MSDS Information
methyl 2,6-dichloro-4-methylnicotinate Usage And Synthesis
Synthesis
2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid

62774-90-7

Iodomethane

74-88-4

methyl 2,6-dichloro-4-methylnicotinate

1013648-04-8

(A) Synthesis of methyl 2,6-dichloro-4-methylnicotinate: 8.05 g (39.1 mmol) of 2,6-dichloro-4-methylnicotinate [Lamm, G. Ger. Offen. (1977), DE 2538950] was dissolved in 100 mL of DMF, followed by the addition of 8.10 g (58.6 mmol) of potassium carbonate. Under stirring conditions, 12.16 mL (27.7 g, 195.4 mmol) of iodomethane was added slowly and dropwise. The reaction mixture was stirred continuously for 6 hours at room temperature. After completion of the reaction, the mixture was poured into crushed ice and extracted twice with EtOAc. The organic phases were combined, washed with water, dried over magnesium sulfate, filtered and the solvent evaporated to give 8.47 g (99% yield) of methyl 2,6-dichloro-4-methylnicotinate as a light yellow solid. Mass spectral data: 219.0 (M+, containing 2Cl).

References[1] Patent: US2009/48238, 2009, A1. Location in patent: Page/Page column 22
[2] Patent: US2009/318467, 2009, A1. Location in patent: Page/Page column 23
[3] Patent: US2012/101079, 2012, A1. Location in patent: Page/Page column 74
[4] Patent: WO2012/52167, 2012, A1. Location in patent: Page/Page column 171-172
[5] Patent: US2017/183342, 2017, A1. Location in patent: Paragraph 0231
methyl 2,6-dichloro-4-methylnicotinate Preparation Products And Raw materials
Raw materials2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid-->Iodomethane-->Potassium carbonate-->N,N-Dimethylformamide
Tag:methyl 2,6-dichloro-4-methylnicotinate(1013648-04-8) Related Product Information
Nicotinic acid 2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid 2,6-Dichloro-4-methylpyridine-3-carboxaldehyde (2,6-dichloro-4-methylpyridin-3-yl)methanol Methyl 6-chloro-4-Methylnicotinate methyl 2-chloro-4-methylpyridine-3-carboxylate