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5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER

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CAS:29682-15-3
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CAS:29682-15-3
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Products Intro: Product Name:5-Bromopyridine-2-carboxylic acid methyl ester
CAS:29682-15-3
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER manufacturers

5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Basic information
Product Name:5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER
Synonyms:Methyl 5-bromopyridine-2-carboxylate, 98+%;5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTE;Methyl 5-bromopicolinate, 5-Bromo-2-(methoxycarbonyl)pyridine;5-broMopicolinic acid Methyl ester;Methyl 5-BroMopyridine-2-carboxylate, 97+%;5-bromopyridin-2-carboxylic acid methyl ester;METHYL 5-BROMO-2-PYRIDINECARBOXYLATE;METHYL 5-BROMOPICOLINATE
CAS:29682-15-3
MF:C7H6BrNO2
MW:216.03
EINECS:681-695-3
Product Categories:Quinolines;Boronic Acid;blocks;Bromides;Carboxes;Pyridines;Pyridine;Pyridine Series
Mol File:29682-15-3.mol
5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Structure
5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Chemical Properties
Melting point 101-103°C
Boiling point 290.9±20.0 °C(Predicted)
density 1.579±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka-0.67±0.10(Predicted)
form powder to crystal
color White to Almost white
Water Solubility Soluble in water.
InChIInChI=1S/C7H6BrNO2/c1-11-7(10)6-3-2-5(8)4-9-6/h2-4H,1H3
InChIKeyJEURNBCYNWNADN-UHFFFAOYSA-N
SMILESC1(C(OC)=O)=NC=C(Br)C=C1
CAS DataBase Reference29682-15-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-36
Safety Statements 26-37
HS Code 29333990
MSDS Information
ProviderLanguage
ALFA English
5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis
UsesMethyl 5-bromopyridine-2-carboxylate is used as an organic chemical synthesis intermediate.
Synthesis
Methanol

67-56-1

5-Bromo-2-pyridinecarboxylic Acid

30766-11-1

5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER

29682-15-3

Example 89 - Preparation of Intermediate 25: The synthesis of Intermediate 25 followed the following general procedure. To a solution of 5-bromopyridine-2-carboxylic acid (50.0 g, 0.247 mol, 1.0 eq.) in anhydrous methanol (400 mL) cooled to 0 °C was added thionyl chloride (107.0 mL, 2.47 mol, 10.0 eq.) dropwise. The reaction mixture was slowly warmed to room temperature and subsequently heated at 50 °C for 12 hours. The reaction process was monitored by thin layer chromatography (TLC) and liquid chromatography-mass spectrometry (LC-MS). After completion of the reaction, the reaction mixture was concentrated under reduced pressure to give a white solid residue. The residue was slowly quenched with saturated sodium bicarbonate solution and the white solid was collected by filtration to afford the target product methyl 5-bromopyridine-2-carboxylate (43.0 g, 80% yield). The product was characterized by mass spectrometry (m/z 216.14) and nuclear magnetic resonance hydrogen spectroscopy (1H NMR, 400 MHz, DMSO): δ 8.86 (d, J=1.9 Hz, 1H), 8.28 (dd, J=8.4,2.4 Hz, 1H), 8.00 (d, J=8.4 Hz, 1H), 3.89 (s, 3H) ppm.

References[1] Patent: WO2018/126072, 2018, A1. Location in patent: Paragraph 0246; 0247
[2] Patent: WO2012/76898, 2012, A1. Location in patent: Page/Page column 64-65
[3] European Journal of Organic Chemistry, 2014, vol. 2014, # 22, p. 4780 - 4784
[4] Patent: WO2016/44662, 2016, A1. Location in patent: Paragraph 00379-00380
[5] Patent: CN103360407, 2016, B. Location in patent: Paragraph 0135-0137
Tag:5-BROMOPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER(29682-15-3) Related Product Information
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