تفاعل #67340

ord-18c23d4b49f94498b2e63b67ed996ec4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe organic layer was washed with brine
  2. 2
    تجفيفdried over sodium sulfate
  3. 3
    تركيزconcentrated
  4. 4
    workup.DISSOLUTIONThe resulting residue was dissolved in 5 mL DMF
  5. 5
    workup.STIRRINGThe reaction stirred at r.t. for 3 h
  6. 6
    أخرىThe organic was dried
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe residue was purified over silica gel (-hexanes-ethyl acetate)

الإجراء التجريبي

(S)-6-amino-3-[(S)-2-(4′-cyano-biphenyl-4-yl)-1-methoxycarbonyl-ethylcarbamoyl]-7-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (1.75 mmol) was dissolved in 5 mL EtOAc, 10 mL water and 15 g sodium bicarbonate added. 2-Chloro-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-acetyl chloride (1.93 mmol) in 5 mL EtOAc was added to the mixture. The resulting mixture stirred at r.t. for 1.5 h. The organic layer was washed with brine, dried over sodium sulfate and concentrated. The resulting residue was dissolved in 5 mL DMF and potassium carbonate (8.75 mmol) added. The reaction stirred at r.t. for 3 h and was poured onto ethyl acetate and water. The organic was dried and concentrated. The residue was purified over silica gel (-hexanes-ethyl acetate) to provide (S)-7-[(S)-2-(4′-Cyano-biphenyl-4-yl)-1-methoxycarbonyl-ethylcarbamoyl]-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6-carboxylic acid tert-butyl ester (931 mg). LC-MS (m/z) 862.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524708B2uspto-grants-2013_09