ChemicalBook--->CAS DataBase List--->1564-49-4

1564-49-4

1564-49-4 Structure

1564-49-4 Structure
IdentificationBack Directory
[Name]

ETHYL 1-METHYL-5-NITROIMIDAZOLE-2-CARBOXYLATE
[CAS]

1564-49-4
[Synonyms]

AKOS 92999
ETHYL 1-METHYL-5-NITROIMIDAZOLE-2-CARBOXYLATE
Ethyl 1-Methyl-5-nitro-1H-iMidazole-2-carboxylate
1H-Imidazole-2-carboxylic acid, 1-methyl-5-nitro-, ethyl ester
[Molecular Formula]

C7H9N3O4
[MDL Number]

MFCD03789116
[MOL File]

1564-49-4.mol
[Molecular Weight]

199.16
Chemical PropertiesBack Directory
[Melting point ]

81-83°C
[Boiling point ]

350.7±34.0 °C(Predicted)
[density ]

1.42±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

-0.95±0.25(Predicted)
[Appearance]

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

ETHYL 1-METHYL-5-NITROIMIDAZOLE-2-CARBOXYLATE(1564-49-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL 1-METHYL-1H-IMIDAZOLE-2-CARBOXYLATE

30148-21-1

ETHYL 1-METHYL-5-NITROIMIDAZOLE-2-CARBOXYLATE

1564-49-4

Step 6a. ethyl 1-methyl-1H-imidazole-2-carboxylate (2.0 g, 13 mmol) was dissolved in 8 mL of concentrated H2SO4, followed by the slow addition of 8 mL of concentrated HNO3. The reaction mixture was stirred at 70 °C for 3 h. The reaction mixture was then extracted with dichloromethane (DCM). After completion of the reaction, the solution was diluted with H2O and the pH was adjusted to 7-8 with aqueous Na2CO3. The reaction mixture was extracted with dichloromethane (DCM) and the organic layers were combined and concentrated. Purification by silica gel column chromatography (eluent: ethyl acetate/petroleum ether) afforded the target compound 1-methyl-5-nitro-1H-imidazole-2-carboxylic acid ethyl ester as a yellow solid (0.9 g, 34.7% yield).ESI-MS m/z = 200.20 [M + H]+.

[References]

[1] Patent: WO2016/183266, 2016, A1. Location in patent: Page/Page column 50
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