تفاعل #1362656

ord-029d52279d184d12a2a79435aea25567

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was heated at 80° C. for 6 hours
  2. 2
    أخرىAfter the completion of the reaction
  3. 3
    workup.DISTILLATIONthe solvent was distilled off
  4. 4
    workup.DISSOLUTIONThe remaining oil was dissolved in ethyl acetate
  5. 5
    استخلاصend product was extracted with a 5 wt % sodium hydrogencarbonate aqueous solution
  6. 6
    أخرىThe resultant aqueous solution was adjusted to a pH of 1 in an ice bath
  7. 7
    workup.ADDITIONby adding 2N hydrochloric acid
  8. 8
    استخلاصextracted with ethyl acetate
  9. 9
    غسيلAn organic layer was washed with a saturated sodium chloride aqueous solution
  10. 10
    تجفيفdried over anhydrous sodium sulfate
  11. 11
    workup.DISTILLATIONthe solvent was distilled off

الإجراء التجريبي

2.0 Grams (7.8 mmol) of 4-hydroxy-6-carboxy-5-methylthiochroman-1,1-dioxide was dissolved in 10 ml of t-amyl alcohol, and 1.0 g (8.6 mmol, 1.1 eq.) of 1-ethyl-5-hydroxypyrazole and 1.8 g (8.6 mmol, 1.1 eq.) of N,N'-dicyclohexylcarbodiimide were added. The mixture was stirred at room temperature for 3 hours. Then, 0.8 g (5.9 mmol) of potassium carbonate was added. The mixture was heated at 80° C. for 6 hours. After the completion of the reaction, the solvent was distilled off. The remaining oil was dissolved in ethyl acetate, and end product was extracted with a 5 wt % sodium hydrogencarbonate aqueous solution. The resultant aqueous solution was adjusted to a pH of 1 in an ice bath by adding 2N hydrochloric acid, and extracted with ethyl acetate. An organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate, and the solvent was distilled off to give 2.0 g (yield 73%) of 4-hydroxy-5-methyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06159904uspto-grants-2000_12