COA of Formula: C9H13NO2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate, is researched, Molecular C9H13NO2, CAS is 2199-44-2, about The reaction of β-aminoenones with α-amino derivatives. Synthesis of 2-functionalized pyrroles. Author is Alberola, Angel; Andres, Jose M.; Gonzalez, Alfonso; Pedrosa, Rafael; Vicente, Martina.
β-Aminoenones react with Et glycinate, α-aminoacetonitrile and α-aminoacetamide hydrochlorides leading to 2-functionalized pyrroles. Although the transamination is a high-yield process, the transformation of the intermediate, in both basic or thermally induced conditions, affords the corresponding pyrroles in poor to moderate yields. Thus, transamination of AcCH:CMeNH2 with EtO2CCH2N+H3 in MeOH gave 89% AcCH:CMeNHCH2CO2Et which on cyclization in EtONa/EtOH gave 33% Et 3,5-dimethyl-2-pyrrolecarboxylate.
This literature about this compound(2199-44-2)COA of Formula: C9H13NO2has given us a lot of inspiration, and I hope that the research on this compound(Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate) can be further advanced. Maybe we can get more compounds in a similar way.
Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com