반응 #84587

ord-88a150245261409481f368308efeb6f7

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONThe aqueous layer of the mixture was poured out
  2. 2
    workup.STIRRINGstirred at 65° C. for 20 min
  3. 3
    여과filtered
  4. 4
    농축the filtrate was concentrated in vacuo
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in EtOAc (100 mL)
  6. 6
    세척the solution was washed with water (30 mL×3) and brine (30 mL×2)
  7. 7
    건조dried over anhydrous Na2SO4 (10 g)
  8. 8
    농축concentrated in vacuo

실험 절차

To a mixture of water (20 mL) and iron powder (697 mg, 12.50 mmol) at 65° C. was added concentrated hydrochloric acid (0.2 mL) dropwise and the mixture was stirred for 15 min. The aqueous layer of the mixture was poured out and a solution of 2-chloro-N-(1-(4-chloro-3-fluorophenyl)-2-methylpropan-2-yl)-4-nitroaniline (446 mg, 1.25 mmol) in MeOH (20 mL) was added to the above processed iron powder. The mixture was adjusted to pH 2-3 and stirred at 65° C. for 20 min. The mixture was then cooled to rt, adjusted to pH 11 with Et3N, and filtered and the filtrate was concentrated in vacuo. The residue was dissolved in EtOAc (100 mL) and the solution was washed with water (30 mL×3) and brine (30 mL×2), dried over anhydrous Na2SO4 (10 g) and concentrated in vacuo to give the crude product, which was used for next step with out further purification. The compound was characterized by the following spectroscopic data:

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09434695B2uspto-grants-2016_09