Analyzing the synthesis route of 1075-34-9

1075-34-9, The synthetic route of 1075-34-9 has been constantly updated, and we look forward to future research findings.

1075-34-9, 5-Bromo-2-methylindole is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

5-bromo-2-methylindole (6.00 g, 28.6 mmol) was dissolved in quinoline (50 mL). Copper cyanide (7.46 g, 83.3 mmol) was added. The mixture was refluxed for 1 hour. The mixture was cooled to room temperature, diluted with EtOAc (500 mL) and washed with ice-cold hydrochloric acid (1M). The organic layer was washed with brine, dried over MgSO4, filtered and evaporated to dryness. Flash chromatography (silica, heptanes:EtOAc 1:1) gave 2-methyl-1H-indole-5-carbonitrile as a brown solid (4.11 g, 83%).

1075-34-9, The synthetic route of 1075-34-9 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; H. Lundbeck A/S; US2012/252853; (2012); A1;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles