تفاعل #80583

ord-4df66f978cd147168989c9d9130ec338

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    درجة الحرارةAfter heating the reaction mixture at 80°-85° C. for 18 hours
  3. 3
    أخرىthe solvent was removed
  4. 4
    workup.DISSOLUTIONThe residue was redissolved in methylene chloride
  5. 5
    غسيلwashed with aqueous sodium bicarbonate and water
  6. 6
    تجفيفdried over sodium sulfate
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated in vacuo
  9. 9
    أخرىThe crude product was chromatographed (silica gel, hexane/ethyl acetate, 6/4)

الإجراء التجريبي

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (700 mg, 2.24 mmol) and sodium bicarbonate (376 mg, 4.48 mmol) in isopropanol (35 mL), 3-chlorophenacyl bromide (1.05 g, 4.48 mmol) was added. After heating the reaction mixture at 80°-85° C. for 18 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was chromatographed (silica gel, hexane/ethyl acetate, 6/4) to give 2-(4-chlorophenyl)-4-(3-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole (525 mg, 53%) as a pale yellow solid: mp 156°-159° C. Anal Calc'd. for C22H16N2SO2Cl2 : C, 59.60, H, 3.69, N, 6.32, S, 7.23. Found: C, 59.43, H, 3.59, N, 6.15, S, 7.16.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05616601uspto-grants-1997_04