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4919-00-0

4919-00-0 Structure

4919-00-0 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P301+P312-P302+P352-P305+P351+P338
[HS Code ]

2933299090
Spectrum DetailBack Directory
[Spectrum Detail]

1H-Imidazole-4-carboxylicacid,5-amino-,methylester(9CI)(4919-00-0)1HNMR
1H-Imidazole-4-carboxylicacid,5-amino-,methylester(9CI)(4919-00-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Imidazole-4-carboxylic acid, 5-nitro-, methyl ester

20271-20-9

1H-Imidazole-4-carboxylicacid,5-amino-,methylester(9CI)

4919-00-0

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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