反应详情

The title compound was prepared by adapting the method for 4-[(3-benzyloxybenzyl)(4-cyanophenyl)amino]-4H-[1,2,4]triazole using the following modifications. To a stirred suspension of NaH (60% dispersion in oil, 0.27 g, 6.78 mmol) in anhydrous DMF (10 mL) was added a solution of 4-[(4-cyanophenyl)amino]-4H-[1,2,4]triazole (1.26 g, 6.78 mmol) in anhydrous DMF (5 mL) and the mixture stirred at r.t. for 0.5 h. A solution of 4-bromo-3-(tetrahydropyran-2-yloxy)benzyl bromide (2.61 g, 7.46 mmol) in anhydrous DMF (5 mL) was then added and the mixture heated at 80-90° C. for 3 h. The mixture was cooled, diluted with EtOAc (50 mL), washed with water (4×100 mL), brine (100 mL) and dried (Na2SO4). Concentration in vacuo and subsequent purification by flash column chromatography [SiO2, EtOAc (100%)] gave 4-[(3-(tetrahydropyran-2-yloxy)-4-bromobenzyl)(4-cyanophenyl)amino]-4H-[1,2,4]triazole as a yellow oil (3.05 g, 99%); δH (270 MHz, CDCl3) 1.61-1.99 (m, 6H), 3.55-3.59 (m, 1H), 3.73 (m, 1H), 4.75 (d, J=14.6, 1H), 4.90 (d, J=14.6, 1H), 5.41 (m, 1H), 6.64 (AA′BB′, 2H), 6.69 (dd, J=8.2, 2.2, 1H), 7.00 (d, J=2.2, 1H), 7.49 (d, J=7.9, 1H), 7.57 (AA′BB′, 2H), 8.15 (s, 2H); LRMS (FAB+) m/z (rel. intensity) 456.1 (54, [C21H20N5O281Br+H]), 454.1 (54, [C21H20N5O279Br+H]); LC-MS (APCI+): tR=2.0 min, m/z 456.1 (94, [C21H20N5O281Br+H]), 454.1 (100, [C21H20N5O279Br+H]); HPLC: tR=2.21 min (94%); HRMS (FAB+): Found 454.08627 C21H21N5O279Br requires 454.08786.

1. customThe title compound was prepared
2. temperaturethe mixture heated at 80-90° C. for 3 h
3. temperatureThe mixture was cooled
4. washwashed with water (4×100 mL), brine (100 mL)
5. dry with materialdried (Na2SO4)
6. concentrationConcentration
7. customin vacuo and subsequent purification by flash column chromatography [SiO2, EtOAc (100%)]