With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.57079-01-3,11-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)undecanoic acid,as a common compound, the synthetic route is as follows.,57079-01-3
Example L1a 11-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-undecanoyl chloride 2.0 g (7.11 mmol) of 11-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-undecanoic acid is mixed with 15.5 ml of thionyl chloride and refluxed for 15 minutes. After cooling, it is mixed with toluene and evaporated to the dry state. 2.13 g (max. 7.11 mmol) of the title compound, which is further reacted without purification, is isolated.
57079-01-3 11-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)undecanoic acid 4618600, apyrrolines compound, is more and more widely used in various fields.
Reference£º
Patent; Klar, Ulrich; Willuda, Joerg; Menrad, Andreas; Bosslet, Klaus; US2005/234247; (2005); A1;,
Pyrroline – Wikipedia
1-Pyrroline | C4H7N – PubChem