ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Pyridine derivatives >IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE

IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE

IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: BeiJing Hwrk Chemicals Limted  
Tel: 0757-86329057 18934348241
Email: sales4.gd@hwrkchemical.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Shanghai Ennopharm Co., Ltd.  
Tel: +86 (21) 6435-5022
Email:
Company Name: Shanghai Aobo pharmaceutical Technology Co., Ltd  
Tel: 86-21-51320499
Email: aobo@aobopharm.com

IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE manufacturers

IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE Basic information
Product Name:IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE
Synonyms:imidazo[3,2-a]pyridine-3-carbaldehyde;IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE;IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE;[1,2-α]PYRIDIN-3-CARBOXALDEHYDE;Imidazo[1,2-a]pyridine-3-carbaldehyde AldrichCPR;3-imidazo[3,2-a]pyridinecarboxaldehyde;Imidazo[1,2-a]pyridine-3-carboxaldehyde (7CI, 8CI, 9CI, ACI);Minodronic Acid Impurity 30
CAS:6188-43-8
MF:C8H6N2O
MW:146.15
EINECS:
Product Categories:blocks;Imidazoles;Pyridines
Mol File:6188-43-8.mol
IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE Structure
IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE Chemical Properties
Melting point 127-129 °C
density 1.24±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka4.15±0.50(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
Hazard Codes Xn
Risk Statements 22
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE Usage And Synthesis
Synthesis
Imidazo[1,2-a]pyridine

274-76-0

N,N-Dimethylformamide

68-12-2

IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE

6188-43-8

Freshly distilled phosphorus trichloride (61 mL, 0.65 mol) was slowly added to N,N-dimethylformamide (120 mL, 1.55 mol) at 2 °C. After controlling the reaction temperature to gradually increase to room temperature, the reaction system was again cooled to 2 °C. Subsequently, a solution of N,N-dimethylformamide (60 mL) of imidazo[1,2-a]pyridine (10 g, 0.085 mol) was added dropwise. The reaction mixture was slowly warmed to 105 °C, followed by further warming to 140 °C. The reaction temperature was stabilized at 120 °C by removing the oil bath. Heating was continued at this temperature for 45 minutes, after which the temperature was reduced to 85 °C and continued for 2.5 hours. Upon completion of the reaction, the mixture was cooled and poured into ice-cooled 5% hydrochloric acid (600 mL) and the pH was adjusted with 20% sodium hydroxide solution to 9. The resulting solution was extracted with dichloromethane (1200 mL) overnight. The organic layer was separated, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was washed with water (5 x 15 mL) and dried again to give 3.49 g of imidazo[1,2-a]pyridine-3-carbaldehyde in 31% yield.

References[1] Farmaco, Edizione Scientifica, 1981, vol. 36, # 12, p. 994 - 1003
[2] Journal of Medicinal Chemistry, 2010, vol. 53, # 9, p. 3454 - 3464
[3] European Journal of Medicinal Chemistry, 2011, vol. 46, # 10, p. 4820 - 4826
[4] Journal of Medicinal Chemistry, 1996, vol. 39, # 14, p. 2856 - 2859
[5] Patent: WO2005/66132, 2005, A1. Location in patent: Page/Page column 89-90
IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE Preparation Products And Raw materials
Raw materialsImidazo[1,2-a]pyridine-->N,N-Dimethylformamide-->Dimethyl sulfoxide
Tag:IMIDAZO[1,2-A]PYRIDIN-3-CARBOXALDEHYDE(6188-43-8) Related Product Information
IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID ETHYL ESTER IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID IMIDAZO[1,2-A]PYRIDINE-6-CARBOXYLIC ACID IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID IMIDAZO[1,2-A]PYRIDIN-2-YLMETHANOL ETHYL IMIDAZO[1,2-A]PYRIDINE-7-CARBOXYLATE 98 Dimethyl 4,5-imidazoledicarboxylate Imidazo[1,2-a]pyridine-6-boronic acid Imidazo[1,2-a]pyridin-5-ylamine Imidazo[1,2-a]pyridine-7-carboxylic acid (9CI) Ethyl Imidazo[1,2-a]pyridine-3-carboxylate IMIDAZO[1,5-A]PYRIDINE-1-CARBOXYLIC ACID ETHYL ESTER ETHYL IMIDAZO[1,2-A]PYRAZINE-2-CARBOXYLATE METHYL IMIDAZO[1,2-A]PYRIDINE-6-CARBOXYLATE Imidazo[1,2-a]pyridine-6-boronic acic pinacol ester Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester Methyl imidazo[1,2-a]pyridine-7-carboxylate