A novel environment-friendly vapour phase synthesis of different classes of nitrogen-containing heterocyclic compounds was developed using non-hazardous, commercially available and low cost feeds. 2-Methyl-8-ethylquinoline (MEQUI) was obtained from 2-ethylaniline (2-ETAN) and ethylene glycol (EG); or chloroethanol (CE), operating at high temperature in the presence of acid-treated K10 montmorillonite or ZnCl2/K10 montmorillonite. At lower temperatures and using copper chromite catalysts, 7-ethylindole (7-ETI) or 5-ethylindole (5-ETI) were obtained from 2-ETAN or 4-ethylaniline (4-ETAN), respectively, and EG; excess of alkylaniline was required to avoid the formation of polyalkylated by-products. Mixing SiO2 with the best copper chromite, made it possible to operate with higher LHSV values, thus improving the yield in alkylindoles. Finally, N-(2-ethylphenyl)pyrrole (EPP) and N-(2-ethylphenyl)pyrrolidine (EPD) were synthesised using a commercial copper chromite catalyst and feeding 2-ETAN and 2,3-dihydrofuran (DHF), EPP being favoured by high temperatures and absence of water in the feed. The possible reaction pathway for each synthesis is proposed, to evidence the key features of the best catalysts identified.