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5-Bromo-1H-benzimidazole

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5-Bromo-1H-benzimidazole manufacturers

5-Bromo-1H-benzimidazole Basic information
Product Name:5-Bromo-1H-benzimidazole
Synonyms:1H-Benzimidazole,5-bromo-(9CI);5-BROMOBENZIMIDAZOLE;5-BROMO-1H-BENZIMIDAZOLE;5-broMo-1H-1,3-benzodiazole;6-bromo-1H-benzimidazole(SALTDATA: FREE);1H-BenziMidazole, 6-broMo-;6-BroMo-1H-benziMidazole 97%;6-Bromobenzimidazole
CAS:4887-88-1
MF:C7H5BrN2
MW:197.03
EINECS:
Product Categories:pharmacetical;Imidazol&Benzimidazole;Building Blocks;C3 to C8;Chemical Synthesis;Pharm intermediate;BENZIMIDAZOLE;Heterocyclic Building Blocks;Imidazoles;New Products for Chemical Synthesis
Mol File:4887-88-1.mol
5-Bromo-1H-benzimidazole Structure
5-Bromo-1H-benzimidazole Chemical Properties
Melting point 130 °C
Boiling point 417.4±18.0 °C(Predicted)
density 1.770±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka11.19±0.30(Predicted)
color White to Yellow to Orange
InChIInChI=1S/C7H5BrN2/c8-5-1-2-6-7(3-5)10-4-9-6/h1-4H,(H,9,10)
InChIKeyGEDVWGDBMPJNEV-UHFFFAOYSA-N
SMILESC1NC2=CC(Br)=CC=C2N=1
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38-36-22
Safety Statements 22-26-36/37/39
WGK Germany 3
HS Code 2933998090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
5-Bromo-1H-benzimidazole Usage And Synthesis
Chemical Propertiesoff-white powder
Uses5-Bromo-1H-benzimidazole is a key intermediate in the synthesis of various organic compounds, especially in the fields of medicine and chemical research.
Synthesis
4-Bromo-1,2-benzenediamine

1575-37-7

Trimethoxymethane

149-73-5

5-Bromo-1H-benzimidazole

4887-88-1

Step 87a: Synthesis of tert-butyl 5-bromo-1H-benzo[d]imidazole-1-carboxylate (compound 0601-187) To a solution of 4-bromo-1,2-benzenediamine (3 g, 16 mmol) in N,N-dimethylformamide (DMF, 22 mL) was added trimethyl orthoformate (44 mL), which was subsequently concentrated. Concentrated hydrochloric acid (1.5 mL) was added and the reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the mixture was diluted with deionized water (200 mL) and the pH was adjusted to 7 with saturated aqueous sodium bicarbonate. the reaction mixture was extracted with ethyl acetate (200 mL) and the organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure to give 5-bromo-1H-benzo[d]imidazole (3.25 g, 100%) as an off-white solid. lc-MS (mass spectrum): m/z 197 [M + H]+. 1H NMR (400 MHz, DMSO-d6) δ 7.33 (t, J = 8.8 Hz, 1H), 7.55 (dd, J1 = 7.6 Hz, J2 = 40 Hz, 1H), 7.79 (d, J = 47.2 Hz, 1H), 8.26 (s, 1H), 12.61 (d, J = 25.6 Hz, 1H ).

References[1] Patent: WO2011/130628, 2011, A1. Location in patent: Page/Page column 228
[2] Patent: US2013/102595, 2013, A1. Location in patent: Paragraph 0580; 0581
[3] Patent: JP2015/187145, 2015, A. Location in patent: Paragraph 0493
[4] Patent: US2009/326029, 2009, A1. Location in patent: Page/Page column 33
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