These common heterocyclic compound, 36947-68-9, name is 2-Isopropyl-1H-imidazole, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. SDS of cas: 36947-68-9
EXAMPLE 11 2-Isopropyl-1-(6-methylergolin-8beta-ylmethyl)imidazole 0.9 g of 50% sodium hydride in an oil was added to a mixture of 4.0 g of 2-isopropylimidazole and 40 ml of dimethylformamide, and the mixture was stirred for 30 minutes. 2.0 g of 6-methylergolin-8beta-ylmethyl tosylate was added to the mixture which was then heated on a water bath for 2 hours. The solvent was distilled off under reduced pressure, and water was added to the residue. The precipitated crystals were filtered, washed with water and purified by silica gel column chromatography (eluted with acetone). The crystals thus obtained were dissolved in methanol, and isopropyl alcohol was added thereto. The mixture was concentrated and allowed to cool to obtain 0.6 g of the titled compound as colorless needles having a melting point of 283-288 C. (with decomposition). NMR (CDCl3) delta: 1.18 (1H, q, J=11.7 Hz), 1.34 (3H, d, J=6.7 Hz), 1.35 (3H, d, J=6.7 Hz), 1.80-3.09 (7H, m), 2.43 (3H, s), 3.37 (1H, dd, J=14.3, 4.4 Hz), 3.80 (2H, d, J=6.8 Hz), 6.65-7.25 (6H, m). Elementary Analysis for C22 H28 N4: Calc’d: C. 75.82; H, 8.10; N, 16.03. Found: C, 76.15; H, 8.39; N, 16.25.
The synthetic route of 2-Isopropyl-1H-imidazole has been constantly updated, and we look forward to future research findings.
Reference:
Patent; Maruko Seiyaku Co., Ltd.; US4713457; (1987); A;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem