تفاعل #83533

ord-2504b72771084d5e8597acea1039705d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with 1N NaOH
  2. 2
    أخرىThe organic layer is evaporated in vacuo to a residue which
  3. 3
    workup.STIRRINGis stirred in 5 ml of tetrahydrofuran for 1 hour
  4. 4
    أخرىevaporated in vacuo to a residue
  5. 5
    استخلاصThe residue is extracted with ethyl acetate-methylene chloride
  6. 6
    غسيلwashed with brine
  7. 7
    تجفيفdried (Na2SO4)
  8. 8
    ترشيحfiltered through hydrous magnesium silicate
  9. 9
    أخرىevaporated in vacuo

الإجراء التجريبي

To a stirred solution of 0.10 g of 10,11-dihydro-10-(4-amino-3-methoxybenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 1 ml of methylene chloride is added 0.06 g of triethylamine followed by 0.05 g of iso-valeryl chloride. The reaction mixture is stirred for 3 hours and then quenched with 1N NaOH. The organic layer is evaporated in vacuo to a residue which is stirred in 5 ml of tetrahydrofuran for 1 hour, then evaporated in vacuo to a residue. The residue is extracted with ethyl acetate-methylene chloride, washed with brine, dried (Na2SO4), filtered through hydrous magnesium silicate and evaporated in vacuo to give 0.15 g of residue which is stirred with ether-hexane to give 0.13 g of light yellow solid. MS(CI): 418(M+H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05624923uspto-grants-1997_04