反应详情

A solution of 6-fluoroquinoxaline-2-carboxylic acid (35 mg, 0.18 mmol) in dimethylformamide (4 mL) was treated with 1,1′-carbonyldiimidazole (29 mg, 0.18 mmol) and the reaction stirred for 16 hours at ambient temperature. After this time the reaction mixture was treated with trans-4-methylcyclohexylamine hydrochloride (27 mg, 0.18 mmol) and N,N-diisopropylethylamine (0.05 mL, 0.29 mmol) and the reaction stirred 2 hours at ambient temperature. The solvent was evaporated to a solid (700 mg). The solid was dissolved in chloroform (10 mL) and added to diethyl ether (30 mL) The organic solution was washed with water (1×25 mL) and brine. The remaining organic solution was dried over anhydrous MgSO4, filtered, and concentrated to a solid (35 mg) HPLC (10 micron silica, 250×20 mm i.d.) of this material using a gradient of chloroform to 10% ethanol (in chloroform) afforded 20 mg (39%) of 434:

1. stirringthe reaction stirred 2 hours at ambient temperature
2. customThe solvent was evaporated to a solid (700 mg)
3. dissolutionThe solid was dissolved in chloroform (10 mL)
4. additionadded to diethyl ether (30 mL) The organic solution
5. washwas washed with water (1×25 mL) and brine
6. dry with materialThe remaining organic solution was dried over anhydrous MgSO4
7. filtrationfiltered
8. concentrationconcentrated to a solid (35 mg) HPLC (10 micron silica, 250×20 mm i.d.) of this material