98416-72-9,With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.98416-72-9,6-Bromo-2-chloro-3-methylquinoxaline,as a common compound, the synthetic route is as follows.
Method B: 4-(4-chlorobenzylideneamino)phenol (0.01 mol) wasdissolved in acetonitrile (50 mL). Anhydrous potassium carbonate(2.0 g) was added to the mixture, which was refluxed for 1 h, then(5, 0.01 mol) was added and the mixture was further refluxed for6 h (monitored by TLC). After completion of the reaction, the mixturewas filtered and the excess of acetonitrile was evaporatedunder reduced pressure to produce the compound, yield; 64%
The synthetic route of 98416-72-9 has been constantly updated, and we look forward to future research findings.
Reference£º
Article; Abbas, Hebat-Allah S.; Al-Marhabi, Aisha R.; Eissa, Sally I.; Ammar, Yousry A.; Bioorganic and Medicinal Chemistry; vol. 23; 20; (2015); p. 6560 – 6572;,
Quinoxaline – Wikipedia
Quinoxaline | C8H6N2 | ChemSpider