Identification | Back Directory | [Name]
1H-Imidazole-4-carboxylicacid,5-amino-,methylester(9CI) | [CAS]
4919-00-0 | [Synonyms]
Methyl 5-Aminoimidazole-4-carboxylate Methyl 5-amino-1H-imidazole-4-carboxylate methyl 4-amino-1H-imidazole-5-carboxylate methyl 4-azanyl-1H-imidazole-5-carboxylate 4-amino-1H-imidazole-5-carboxylic acid methyl ester 1H-Imidazole-4-carboxylic acid, 5-amino-, methyl ester 1H-Imidazole-4-carboxylicacid,5-amino-,methylester(9CI) | [Molecular Formula]
C5H7N3O2 | [MOL File]
4919-00-0.mol | [Molecular Weight]
141.13 |
Chemical Properties | Back Directory | [Boiling point ]
397.0±22.0 °C(Predicted) | [density ]
1.395±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
solid | [pka]
11.51±0.10(Predicted) | [color ]
Off-white to light yellow | [InChI]
InChI=1S/C5H7N3O2/c1-10-5(9)3-4(6)8-2-7-3/h2H,6H2,1H3,(H,7,8) | [InChIKey]
DESDXDWZSJRLDB-UHFFFAOYSA-N | [SMILES]
C1NC(N)=C(C(OC)=O)N=1 |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 5-amino-1H-imidazole-4-carboxylic acid methyl ester from 5-nitro-1H-imidazole-4-carboxylic acid methyl ester: 5-nitro-1H-imidazole-4-carboxylic acid methyl ester (1.24 g, 7.55 mmol) was dissolved in a 1:1 solvent mixture of ethanol:methanol (60 ml) and 10% palladium/carbon catalyst was added. The hydrogenation reaction was carried out under hydrogen balloon atmosphere. After 4 hours of reaction, the catalyst was removed by filtration, the filtrate was concentrated and azeotroped with ethanol to remove residual water. The resulting product was ground with ethyl acetate and dried to give methyl 5-amino-1H-imidazole-4-carboxylate as a white solid (0.98 g, 96% yield). The product was characterized by 1H NMR (400 MHz, DMSO): δ 12.0 (1H, brs), 7.32 (1H, s), 5.56 (2H, s), 3.70 (3H, s). Mass spectrum (ES+) showed m/z 142 ([M+H]+). | [References]
[1] Patent: WO2005/49613, 2005, A1. Location in patent: Page/Page column 44 [2] Zhurnal Obshchei Khimii, 1959, vol. 29, p. 2401;engl.Ausg.S.2366 |
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parabiochem
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