تفاعل #678527

ord-b2d5a6cb376e42f7ab91332e28db0afd

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe resulting mixture was stirred at room temperature for 24 h
  2. 2
    workup.STIRRINGAfter 30 min stirring
  3. 3
    أخرىthe layers were separated
  4. 4
    استخلاصThe aqueous layer was extracted with CH2Cl2 (100 mL)
  5. 5
    غسيلThe combined organic layer was washed with brine (100 mL)
  6. 6
    تجفيفdried (Na2SO4)
  7. 7
    ترشيحfiltered
  8. 8
    أخرىThe solvent was removed by roto-evaporator, Et2O (10 mL)
  9. 9
    workup.ADDITIONhexane (150 mL) were added to the resulting residue
  10. 10
    أخرىresulting in the formation of a white solid, which
  11. 11
    أخرىwas collected
  12. 12
    غسيلwashed with 5% Et2O/hexane
  13. 13
    أخرىdried

الإجراء التجريبي

To a solution of 6-fluoroindoline (9.36 g, 68 mmol) in CH2Cl2 (100 mL) was added 1-Boc-4-piperidone (13.6 g, 68 mmol). The resulting mixture was stirred at room temperature for 1 h and NaBH(OAc)3 (18 g, 85 mmol, 1.25 equiv) was added. The resulting mixture was stirred at room temperature for 24 h and was then poured slowly to a vigorously stirred Na2CO3(aq). After 30 min stirring, the layers were separated. The aqueous layer was extracted with CH2Cl2 (100 mL). The combined organic layer was washed with brine (100 mL), dried (Na2SO4), and filtered. The solvent was removed by roto-evaporator, Et2O (10 mL) and then hexane (150 mL) were added to the resulting residue. The mixture was allowed to stand, resulting in the formation of a white solid, which was collected and washed with 5% Et2O/hexane and then dried. This was repeated to yield three crops of tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09238658B2uspto-grants-2016_01