ChemicalBook--->CAS DataBase List--->173530-73-9

173530-73-9

173530-73-9 Structure

173530-73-9 Structure
IdentificationBack Directory
[Name]

Ethyl8-hydroxy-2-MethyliMidazo[1,2-a]pyridine-3-carboxylate
[CAS]

173530-73-9
[Synonyms]

Ethyl8-hydroxy-2-MethyliMidazo[1,2-a]pyridine-3-carboxylate
8-Hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester
Imidazo[1,2-a]pyridine-3-carboxylic acid, 8-hydroxy-2-methyl-, ethyl ester
[Molecular Formula]

C11H12N2O3
[MDL Number]

MFCD14540723
[MOL File]

173530-73-9.mol
[Molecular Weight]

220.22
Chemical PropertiesBack Directory
[density ]

1.31±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

4.90±0.30(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl8-hydroxy-2-MethyliMidazo[1,2-a]pyridine-3-carboxylate(173530-73-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

8-BENZYLOXY-2-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER

96428-50-1

Ethyl8-hydroxy-2-MethyliMidazo[1,2-a]pyridine-3-carboxylate

173530-73-9

Example 3A Synthesis of ethyl 8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxylate: 31.45 g (101.3 mmol) of ethyl 8-(benzyloxy)-2-methylimidazo[1,2-a]pyridine-3-carboxylate was dissolved in 2 L of ethyl acetate and 3.15 g of 10% Pd/C catalyst was added. The mixture was stirred at room temperature and atmospheric pressure for 5 hours in a hydrogen atmosphere. Upon completion of the reaction, the mixture was filtered through diatomaceous earth and the filter cake was washed well with ethyl acetate/methanol (volume ratio not specified). The filtrates were combined and concentrated to dryness under reduced pressure to give 21.94 g ethyl 8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxylate in 98% yield and 99% purity. The product was analyzed by LC-MS (Method 1): retention time (Rt) = 0.61 min, mass spectrum (ESpos): m/z = 221 [M + H]+. 1H NMR (400 MHz, DMSO-d6) δ: 1.36 (t, 3H), 2.60 (s, 3H), 4.36 (q, 2H), 6.78 (d, 1H), 6.98 (t , 1H), 8.73 (d, 1H), 10.60 (br s, 1H).

[References]

[1] Patent: US2014/128386, 2014, A1. Location in patent: Paragraph 0994; 0995; 0996; 0997; 0997
[2] Patent: US2017/57954, 2017, A1. Location in patent: Paragraph 0625; 0626; 0627; 0628; 0629
[3] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999, vol. 38, # 6, p. 635 - 638
[4] Patent: US2017/217954, 2017, A1
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