(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile
(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile Basic information
- Product Name:
- (1-Methyl-1H-benzoimidazol-2-yl)acetonitrile
- Synonyms:
-
- 1H-Benzimidazole-2-acetonitrile,1-methyl-(9CI)
- 1-Methyl-1H-benzimidazole-2-acetonitrile
- 1-Methyl-2-(cyanomethyl)-1H-benzoimidazole
- (1-Methyl-1H-benzoimidazol-2-yl)acetonitrile
- 2-(1-methylbenzimidazol-2-yl)acetonitrile
- 2-(1-methylbenzimidazol-2-yl)ethanenitrile
- 1-Methyl-2-benziMidazolylacetonitrile
- 2-(1-Methyl-1H-benzo[d]iMidazol-2-yl)acetonitrile
- CAS:
- 2735-62-8
- MF:
- C10H9N3
- MW:
- 171.2
- Product Categories:
-
- BENZIMIDAZOLE
- Mol File:
- 2735-62-8.mol
(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- Off-white to light brown Solid
- EPA Substance Registry System
- 1-Methyl-2-benzimidazoleacetonitrile (2735-62-8)
(1-Methyl-1H-benzoimidazol-2-yl)acetonitrile Usage And Synthesis
Synthesis
4414-88-4
77-78-1
2735-62-8
The general procedure for the synthesis of 2-(1-methyl-1H-benzo[d]imidazol-2-yl)acetonitrile from 2-cyanomethylbenzimidazole and dimethyl sulfate was as follows: 1.2 equivalents of dimethyl sulfate was added drop-wise to a mixture containing benzimidazol-2-ylacetonitrile (3b) and 1.1 equivalents of aqueous sodium hydroxide, and the temperature of the reaction was maintained at 30 °C, with continuous stirring for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and the precipitate was collected by filtration, washed several times with deionized water and subsequently dried. The yield of the final product was 78%.
References
[1] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 9, p. 2053 - 2059
[2] Synthetic Communications, 2007, vol. 37, # 13, p. 2259 - 2266
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 1, p. 238 - 252
[4] Angewandte Chemie - International Edition, 2014, vol. 53, # 27, p. 7079 - 7084
[5] Angew. Chem., 2014, vol. 126, # 27, p. 7199 - 7204,6
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