تفاعل #44175

ord-331648d55fa94256b6a3643d83c4757a

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزthen concentrated under vacuum
  2. 2
    غسيلeluted with methanol
  3. 3
    تركيزThe combined basic fractions were concentrated under vacuum
  4. 4
    workup.DISSOLUTIONThe residue, (10 mg) was then dissolved in DCM (1 mL)
  5. 5
    workup.STIRRINGThe mixture was stirred for 1 h
  6. 6
    تركيزthen concentrated under vacuum
  7. 7
    أخرىpurified by preparative mass-directed hplc

الإجراء التجريبي

A solution of (R)-(1,1-dimethylethyl 2-{[(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)amino]methyl}-1-pyrrolidinecarboxylate in methanol was treated with a solution of hydrogen chloride in ether (1M). The resulting mixture was stirred 30 minutes then concentrated under vacuum and then loaded onto an ion-exchange cartridge (SCX-2) and eluted with methanol followed by ammonia in methanol (1 M). The combined basic fractions were concentrated under vacuum. The residue, (10 mg) was then dissolved in DCM (1 mL) and treated with triphosgene (23 mg, 0.3 eq.), diisopropylamine (4 uL, 3 eq.). The mixture was stirred for 1 h then concentrated under vacuum and purified by preparative mass-directed hplc to afford the title compound (3.1 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07732600B2uspto-grants-2010_06