Condensed 1,3,5-triazepines – IV. The synthesis of 2,3-dihydro-1H-imidazo[1,2-a][1,3,5]benzotriazepines was written by Agai, B.;Hornyak, G.;Lempert, K.;Simig, G.. And the article was included in Periodica Polytechnica, Chemical Engineering in 1982.Product Details of 24134-26-7 This article mentions the following:
Imidazobenzotriazepines I (R = H, Bu; R1 = H, Me; R2 = H, 8-Cl, 8-BuNHCO) were prepared by cyclizing imines II (R3 = NH2) (III), obtained by catalytic hydrogenation of II (R3 = NO2), with R1C(OEt)3. I (R = H, Bu; R1 = SMe; R2 = H, 8-MeO, 8-MeO2C, 8-Cl, 9-Cl, 8-BuNHCO) were prepared by S-methylating the thiones prepared by cyclizing III with Cl2CS. I (R = H, Bu; R1 = NHBu, morpholino, 4-methylpiperazino; R2 = H, 8-MeO, 8-Cl, 9-Cl, 8-BuNHCO) were obtained by aminating I (R1 = SMe). In the experiment, the researchers used many compounds, for example, 2,3-Dihydro-1H-benzo[d]imidazo[1,2-a]imidazole (cas: 24134-26-7Product Details of 24134-26-7).
2,3-Dihydro-1H-benzo[d]imidazo[1,2-a]imidazole (cas: 24134-26-7) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Product Details of 24134-26-7
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem