反应详情

温度

0 °C

A solution of 5-(1H-1-indolylmethyl)-3-methylisoxazole (212 mg, 1.0 mmol) in 10 mL diethyl ether was added to oxalyl chloride (254 mg, 2.0 mmol) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 3 hours and then the reaction solvent was evaporated. The residue was dissolved in 5 mL tetrahydrofuran and then the 3-methyl-5-isothiazolamine (114 mg, 1.0 mmol) and triethylamine (1 mL) in 10 mL tetrahydrofuran was added dropwise. The mixture was stirred for 10 hours and then 1 N NaOH (4 mL) was added to the reaction flask dropwise. The mixture was extracted three times with a total of 60 mL of tetrahydrofuran, the organic phase was dried using anhydrous magnesium sulfate and filtered, and the filtrate was concentrated in vacuum. The residue was crystallized from methanol. Yield: 0.27 g, 71%.

1. customthe reaction solvent was evaporated
2. dissolutionThe residue was dissolved in 5 mL tetrahydrofuran
3. stirringThe mixture was stirred for 10 hours
4. extractionThe mixture was extracted three times with a total of 60 mL of tetrahydrofuran
5. customthe organic phase was dried
6. filtrationfiltered
7. concentrationthe filtrate was concentrated in vacuum
8. customThe residue was crystallized from methanol