تفاعل #9685

ord-a7d2367f51754c8a9d86866ac0fbbed9

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةbefore being heated
  2. 2
    درجة الحرارةat reflux overnight
  3. 3
    تركيزwas concentrated under reduced pressure
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
  5. 5
    غسيلwashed with 2 N aqueous hydrochloric acid solution and water
  6. 6
    تجفيفdried (Na2SO4)
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىThe residue was purified by flash chromatography on silica gel
  9. 9
    غسيلeluting with 85:15 hexanes/ethyl acetate

الإجراء التجريبي

2-Amino-4-(trifluoromethyl)phenol (250 mg, 1.41 mmol) and 1-bromo-4-isothio-cyanatobenzene (302 mg, 1.41 mmol) were stirred in ethyl alcohol at ambient temperature for 18 h. The flask was charged with 1-[3-(dimethylamino)propyl]-3-ethylcarhodiimide hydrochloride (EDCI) (405 mg, 2.12 mmol), and the mixture was stirred for 2 h before being heated at reflux overnight. The reaction was allowed to cool to rt and was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with 2 N aqueous hydrochloric acid solution and water, dried (Na2SO4), and concentrated in vacuo. The residue was purified by flash chromatography on silica gel, eluting with 85:15 hexanes/ethyl acetate to provide the title compound (315 mg, 62%). LC-MS m/z 357.1 (MH+), retention time 4.20 minutes.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091228B2uspto-grants-2006_08