تفاعل #78616

ord-3754449e837d402481b72d5dd11f5505

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThen the mixture was washed with 40 mL of saturated sodium hydrogen carbonate solution
  2. 2
    تجفيفthe organic phase was dried with sodium sulfate
  3. 3
    workup.DISTILLATIONthe solvent was distilled off
  4. 4
    درجة الحرارةheated
  5. 5
    workup.WAITto boiling for one hour
  6. 6
    workup.DISTILLATIONThen the solvent was distilled off in vacuo
  7. 7
    غسيلthe organic phase was washed with 100 mL of water
  8. 8
    تجفيفdried with sodium sulfate
  9. 9
    أخرىAfter the solvent had been removed in vacuo

الإجراء التجريبي

A mixture of 1.54 g (3.85 mmol) of 2-methoxymethylthiazolo[5,4-b]pyridin-6-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide and 4.3 mL (4.3 mmol) of a 1 molar solution of boron tribromide in methylene chloride was dissolved in a further 30 mL of methylene chloride and stirred for 5 hours at room temperature. Then the mixture was washed with 40 mL of saturated sodium hydrogen carbonate solution, the organic phase was dried with sodium sulfate, and the solvent was distilled off. The crude product (1.9 g) was taken up in 15.0 mL of N,N-diisopropylethylamine, mixed with 0.50 g (4.2 mmol) of 4-aminobenzonitrile, and heated to boiling for one hour. Then the solvent was distilled off in vacuo, the crude product was taken up in 100 mL of methylene chloride, the organic phase was washed with 100 mL of water, and dried with sodium sulfate. After the solvent had been removed in vacuo, the crude product obtained was purified by flash chromatography (silica gel; ethyl acetate/petroleum ether=35:65 to 1:1) and evaporated down again in vacuo. Yield: 0.45 g (24% of theory) of yellow amorphous solid; Rf value: 0.34 (silica gel; ethyl acetate/petroleum ether=1:1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06710055B2uspto-grants-2004_03