تفاعل #5911
ord-876c69db2b8146499f39252eada8512a
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGthe mixture is stirred for a further 14 hours
- 2استخلاصhydrolyzed with 300 ml of 1N phosphoric acid and the resulting mixture is extracted several times with methyl tert-butyl ether
- 3تجفيفThe organic phases are dried over sodium sulfate
- 4أخرىevaporated down under reduced pressure
- 5workup.STIRRINGAfter the mixture has been stirred for 30 minutes at room temperature
- 6workup.STIRRINGthe whole is stirred for 14 hours
- 7استخلاصextracted with diethyl ether
- 8تجفيفThe ether phase is dried over sodium sulfate
- 9أخرىevaporated down
- 10أخرىthe residue is purified by column chromatography
الإجراء التجريبي
1.75 g (10.8 mmol) of N,N'-carbonylbisimidazole is added to a solution of 1.88 g (10 mmol) of 6-imidazolylsalicylic acid in 30 ml of tetrahydrofuran. After the mixture has been stirred for 30 minutes at room temperature, 9.9 mmol of N-hydroxypyrazole is added and the mixture is stirred for a further 14 hours. The reaction mixture is then hydrolyzed with 300 ml of 1N phosphoric acid and the resulting mixture is extracted several times with methyl tert-butyl ether. The organic phases are dried over sodium sulfate and evaporated down under reduced pressure. The residue is taken up in 40 ml of dimethylformamide, and 280 mg of sodium hydride (85% strength in paraffin, 10 mmol) is added. After the mixture has been stirred for 30 minutes at room temperature, 1.58 g (9 mmol) of 1-chloro-3,5-dimethoxy-s-triazine is added and the whole is stirred for 14 hours. The batch is introduced into 300 ml of 0.1N phosphoric acid, and extracted with diethyl ether. The ether phase is dried over sodium sulfate and evaporated down, and the residue is purified by column chromatography.