تفاعل #80632

ord-b3dd10895ff747d79bcb76f20cd8bfa5

معادلة التفاعل

CC(=O)[O-].[Na+]
sodium acetate
Cc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(C)(=O)=O)cc2)cn1
solution
Cc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(C)(=O)=O)cc2)cn1
2-methyl-5-[1-[4-(methylsulfonyl)phenyl]-4-trifluoromethyl-1H-imidazol-2-yl]pyridine
CCC[CH2][Mg][Cl]
n-BuMgCl
NOS(=O)(=O)O
hydroxylamine-O-sulfonic acid
CCB(CC)CC
triethylborane
Cc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)cn1
4-[2-(6-methylpyridin-3-yl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide
المردود 12.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe ice bath was removed
  2. 2
    workup.STIRRINGthe solution was stirred for 2 hours
  3. 3
    أخرىwas recooled to 0° C.
  4. 4
    workup.STIRRINGAfter stirring for 1 hour
  5. 5
    درجة الحرارةthe reaction was heated
  6. 6
    درجة الحرارةto reflux for 72 hours
  7. 7
    workup.STIRRINGAfter stirring for 5 minutes
  8. 8
    workup.STIRRINGthe mixture stirred for 24 hours
  9. 9
    استخلاصextracted with ether
  10. 10
    تجفيفThe ethereal layer was dried over sodium sulfate
  11. 11
    ترشيحfiltered
  12. 12
    تركيزconcentrated
  13. 13
    أخرىThe crude solid (13.3 g) was chromatographed (silica gel, hexane/isopropanol, 7/3)

الإجراء التجريبي

To a clear solution of Example 33 (2.4 g, 6.3 mmol) in tetrahydrofuran (60 ml) at 0° C., n-BuMgCl (2M solution in THF, 15.7 ml, 31.5 mmol) was added over 10 minutes. After stirring for additional 20 minutes, the ice bath was removed and the solution was stirred for 2 hours. The reaction mixture was recooled to 0° C. and triethylborane (1M solution in THF, 38 ml, 38 mmol) was added. After stirring for 1 hour, the reaction was heated to reflux for 72 hours. The reaction mixture was cooled to room temperature and treated with aqueous sodium acetate (5.5 g in 22 ml water). After stirring for 5 minutes, solid hydroxylamine-O-sulfonic acid (5.5 g) was added and the mixture stirred for 24 hours. The reaction mixture was diluted with water and extracted with ether. The ethereal layer was dried over sodium sulfate, filtered and concentrated. The crude solid (13.3 g) was chromatographed (silica gel, hexane/isopropanol, 7/3) to give 4-[2-(6-methylpyridin-3-yl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide (298 mg, 12%): mp (DSC) 203° C. Anal. Calc'd. for C16H13N4SO2F3 0.25H2O: C, 49.68, H, 3.52 N, 14.48, S, 8.29. Found: C, 49.88, H, 3.39, N, 13.94, S, 8.47.

المصدر

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