反应详情

To a 10 mL reaction vessel containing (5-fluoro-6-methoxybenzothiazol-2-yl) acetonitrile (100 mg, 0.45 mmol) in 4 mL of anhydrous dichloromethane were added cyclopropane carbonyl chloride (21 μL, 0.231 mmol), 1.35 equivalents of triethylamine (85 μL) and a catalytic amount of DMAP (10 mg). The reaction was agitated at room temperature for approximately 3 hrs. At this point the solvent was evaporated and CCl4 (4 mL), 2.5 equivalents of polystyrene resin bound triphenylphosphine (725 mg, 1.55 mmol/g), and triethylamine (85 μL) were added. After agitation at 65° C. for a minimum of 3 hrs, the reaction mixture was concentrated. Ethanol (4 mL) and hydrazine monohydrate (40 μL, 1.8 equivalents) were then added and the mixture was refluxed for approximately 6 hrs. Several drops of concentrated HCl were then added to ensure complete cyclization of the pyrazole ring. After completion of the reaction, the solids were removed by filtration and the resin was washed three times with 10% methanol in dichloromethane. The filtrate was then concentrated and purified by flash column chromatography eluting with CH2Cl2:MeOH=50:1 to yield 40 mg (29%) of the title compound as a cream coloured solid. MS (m/z, ES+): 305.1 (M+1, 100%)

1. customTo a 10 mL reaction vessel
2. customAt this point the solvent was evaporated
3. additionwere added
4. concentrationAfter agitation at 65° C. for a minimum of 3 hrs, the reaction mixture was concentrated
5. temperaturethe mixture was refluxed for approximately 6 hrs
6. customAfter completion of the reaction
7. customthe solids were removed by filtration
8. washthe resin was washed three times with 10% methanol in dichloromethane
9. concentrationThe filtrate was then concentrated
10. custompurified by flash column chromatography
11. washeluting with CH2Cl2