Analyzing the synthesis route of 10242-02-1

10242-02-1, 10242-02-1 5-Methyl-1H-indole-3-carboxylic acid 18385291, aindole-building-block compound, is more and more widely used in various fields.

10242-02-1, 5-Methyl-1H-indole-3-carboxylic acid is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: Following the above procedure, the crude reaction mixture was diluted with MeOH and cooled to 0C. Then SOCl2 (36 muL, 0.5 mmol) was added and stirred for 3 h at room temperature. Additional MeOH was added and the reaction mixture was heated to reflux for 6 h. The resulting mixture was quenched with H2O and extracted with EtOAc (3x). The combined organic layers were dried over MgSO4 and concentrated under reduced pressure. The resulting crude residue was purified by preparative TLC (hexane:EtOAc = 7:3) to afford the desired products 5a-b.

10242-02-1, 10242-02-1 5-Methyl-1H-indole-3-carboxylic acid 18385291, aindole-building-block compound, is more and more widely used in various fields.

Reference£º
Article; Yoo, Woo-Jin; Nguyen, Thanh V. Q.; Guiteras Capdevila, Montse; Kobayashi, Shu; Heterocycles; vol. 90; 2; (2015); p. 1196 – 1204;,
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