21296-93-5, 5-Chloro-2,3-dimethyl-1H-indole is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated
Organic urea catalyst (2S) -2-[[[[[3,5-bis (trifluoromethyl) phenyl] amino] oxomethyl] amino] -N- (diphenylmethyl) -N, 3,3-trimethylbutyramide (44.8 mg, 0.08 mmol), 2,3-dimethyl-5-chloroindole (71.8 mg, 0.4 mmol), diphenyl phosphate (9.8 mg, 0.04 mmol) and A molecular sieve (199.5 mg) was dissolved in n-hexane (16 mL), and then ethyl trifluoropyruvate (106 muL, 0.8 mmol) was added. The reaction was carried out at room temperature for 42.5 hours. The reaction equation is as follows:The reaction solution was filtered through silica gel, rinsed with ether, and concentrated. Silica gel column chromatography was used to obtain 112 mg of a solid product. The calculated yield was 80%. The measured er value was 93: 7, and n-hexane / dichloromethane (1: 1) was used. ) Recrystallization, mother liquor was concentrated to obtain 100 mg of liquid product, the calculated yield was 72%, and the er value was 96: 4., 21296-93-5
The synthetic route of 21296-93-5 has been constantly updated, and we look forward to future research findings.
Reference:
Patent; Hong Kong University Of Science And Technology Shenzhen Institute; Sun Jianwei; Ma Dengke; (35 pag.)CN110437126; (2019); A;,
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