تفاعل #49880

معادلة التفاعل

phosgene

3-(2,4,6-trimethylphenylsulfonyl)pyrazole

toluene

toluene

→

title compound

المردود 89.0%

1-(Dipropylcarbamoyl)-3-(2,4,6-trimethylphenylsulfonyl)pyrazole

المردود 89.0%

ظروف التفاعل

المعالجة

1. 1
   تركيزThe mixture was concentrated by evaporation under reduced pressure
2. 2
   workup.ADDITION97 mg of triethylamine and 89 mg of diisopropylamine were added, in that order, to the oily residue
3. 3
   workup.ADDITIONafter which it was diluted with diethyl ether
4. 4
   غسيلThe ethereal solution was washed with 1N aqueous hydrochloric acid, with an aqueous solution of sodium hydrogencarbonate and with water, in that order
5. 5
   تجفيفwas then dried over anhydrous sodium sulfate
6. 6
   أخرىThe solvent was removed by distillation under reduced pressure
7. 7
   أخرىthe resulting residue was purified by column chromatography through silica gel
8. 8
   غسيلeluted with a 6:1 by volume mixture of hexane and ethyl acetate

الإجراء التجريبي

2 ml of a 1.98M solution of phosgene in toluene were added to a solution of 200 mg of 3-(2,4,6-trimethylphenylsulfonyl)pyrazole [prepared as described in step (2) above] in 1 ml of toluene, and the resulting solution was heated at 60° C. for 1 hour. The mixture was concentrated by evaporation under reduced pressure, and then 97 mg of triethylamine and 89 mg of diisopropylamine were added, in that order, to the oily residue. The reaction mixture was then stirred at ambient temperature for 20 minutes, after which it was diluted with diethyl ether. The ethereal solution was washed with 1N aqueous hydrochloric acid, with an aqueous solution of sodium hydrogencarbonate and with water, in that order, and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, eluted with a 6:1 by volume mixture of hexane and ethyl acetate, to afford 268 mg (yield 89%) of the title compound, melting at 64°-65° C.

المصدر