تفاعل #2081846

ord-5bd85b0d62794adcaad443c89c95e4d2

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat 0° C.
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 1 hr
  3. 3
    استخلاصthe mixture was extracted with ethyl acetate
  4. 4
    غسيلThe ethyl acetate layer was washed with saturated brine
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    تركيزconcentrated

الإجراء التجريبي

To a suspension of sodium hydride (60%, in oil, 0.51 g) in N,N-dimethylformamide (15 ml) was slowly added ethyl 7-nitro-1H-indole-2-carboxylate (2.50 g) at 0° C., and the mixture was stirred for 30 min. Chloromethyl methyl ether (1.00 ml) was added to the reaction mixture over 20 min at 0° C., and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (2.29 g, yield 77%) as pale-yellow crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio). melting point 62-63° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07652133B2uspto-grants-2010_01