ChemicalBook--->CAS DataBase List--->106429-57-6

106429-57-6

106429-57-6 Structure

106429-57-6 Structure
IdentificationBack Directory
[Name]

5-CARBOXYBENZIMIDAZOLONE METHYL ESTER
[CAS]

106429-57-6
[Synonyms]

5-CARBOXYBENZIMIDAZOLONE METHYL ESTER
Methyl 2-Oxo-2,3-dihydrobenzimidazole-5-carboxylate
Methyl 2-oxo-1,3-dihydro-1,3-benzodiazole-5-carboxylate
methyl 2-oxo-2,3-dihydro-1H-1,3-benzodiazole-5-carboxylate
Methyl 2-oxo-2,3-dihydro-1H-benzo[d]iMidazole-5-carboxylate
methyl 2-oxo-2,3-dihydro-1H-1,3-benzimidazole-5-carboxylate
2-Oxo-2,3-dihydro-1H-benzoimidazole-5-carboxylic acid methyl ester
1H-Benzimidazole-5-carboxylic acid, 2,3-dihydro-2-oxo-, methyl ester
1H-Benzimidazole-5-carboxylicacid,2,3-dihydro-2-oxo-,methylester(9CI)
[EINECS(EC#)]

200-110-4
[Molecular Formula]

C9H8N2O3
[MDL Number]

MFCD08457979
[MOL File]

106429-57-6.mol
[Molecular Weight]

192.17
Chemical PropertiesBack Directory
[Melting point ]

312-313°
[Boiling point ]

221.2±19.0 °C(Predicted)
[density ]

1.325±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

11.54±0.30(Predicted)
[Appearance]

Light brown to gray Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

5-CARBOXYBENZIMIDAZOLONE METHYL ESTER(106429-57-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 3,4-diaminobenzoate

36692-49-6

1,1'-Carbonyldiimidazole

530-62-1

5-CARBOXYBENZIMIDAZOLONE METHYL ESTER

106429-57-6

Methyl 3,4-diaminobenzoate (5.00 g, 30.1 mmol) was dissolved in THF (40 mL) at 0 °C, followed by the addition of N,N'-carbonyldiimidazole (7.32 g, 45.1 mmol). The reaction mixture was stirred at 0 °C for 16 h and gradually warmed up to 23 °C. Upon completion of the reaction, 1M HCl aqueous solution (50 mL) was slowly added followed by water (70 mL) at 0 °C and stirring was continued for 1 hour. The resulting precipitate was collected by filtration and dried under reduced pressure for 18 h to afford methyl 2-oxo-2,3-dihydro-1H-benzo[d]imidazole-5-carboxylate (5.45 g, 94% yield), and the product could be used for subsequent reactions without further purification. Mass spectrum (ESI/CI): calculated value C9H8N2O3, 192.1; measured value m/z 193.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ: 11.01 (s, 1H), 10.84 (s, 1H), 7.63 (dd, J=8.2,1.6Hz, 1H), 7.47 (s, 1H). 7.02 (d, J=8.2Hz, 1H), 3.82 (s, 3H).

[References]

[1] Patent: WO2009/134750, 2009, A1. Location in patent: Page/Page column 139
[2] Journal of Medicinal Chemistry, 2006, vol. 49, # 12, p. 3719 - 3742
[3] Patent: US2010/249124, 2010, A1. Location in patent: Page/Page column 62
[4] Cell Chemical Biology, 2018, vol. 25, # 6, p. 677 - 12,690
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