تفاعل #59073

ord-c0ac4d88de934674ab369f7e17615636

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for 3 h
  2. 2
    تركيزThe reaction mixture was then concentrated to half its volume
  3. 3
    استخلاصIt was then extracted with ethyl acetate
  4. 4
    غسيلthe organic layer was washed with brine
  5. 5
    تجفيفdried with sodium sulfate
  6. 6
    أخرىThe crude material was then purified on preparative chromatography

الإجراء التجريبي

To 3-(tert-butyl)benzenisothiocyanate (1 eq) in methanol was added N-{4-[3-amino-4-(methylamino)phenoxy](2-pyridyl)}[(2-morpholin-4-ylethyl)amino]carboxamide (1 eq) and the resulting mixture was stirred at ambient temperature for 16 h. LC/MS showed formation of corresponding thiourea. To this was added anhydrous ferric chloride (1.5 eq) and stirred for 3 h. The reaction mixture was then concentrated to half its volume and brought to neutral pH with 1N sodium hydroxide. It was then extracted with ethyl acetate and the organic layer was washed with brine and dried with sodium sulfate. The crude material was then purified on preparative chromatography to yield N-[4-({2-[(3 -tert-butylphenyl)amino]-1-methyl-1H-benzimidazol-5-yl}oxy)pyridin-2-yl]-N′-(2-morpholin-4-ylethyl)urea. MS: MH+=544.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07423150B2uspto-grants-2008_09