تفاعل #40895

ord-89b9fac623f644f58e5b221f3871bc84

المذيبات

ظروف التفاعل

درجة الحرارة
-5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGby stirring at room temperature for 3 hours
  2. 2
    استخلاصfollowed by extraction with ethyl acetate
  3. 3
    غسيلThe organic layer was washed in turn with an aqueous saturated sodium hydrogen carbonate solution, water and saturated saline
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    تركيزconcentrated
  6. 6
    أخرىThe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5→91:9)

الإجراء التجريبي

To a chloroform (0.8 mL) solution of dimethyl disulfide (30 mg), sulfuryl chloride (34 mg) was added at −15° C. and the mixture was stirred at −5° C. for 1.5 hours. To the reaction mixture, a chloroform (0.5 mL) solution of the compound prepared in Example 43, namely, ethyl 4-{7-bromo-1-[2-(ethyloxy)-2-oxoethyl]-1H-indol-3-yl}butanoate (100 mg) was added at −78° C., followed by stirring at room temperature for 3 hours. To the reaction mixture, an aqueous saturated sodium hydrogen carbonate solution was added under ice cooling, followed by extraction with ethyl acetate. The organic layer was washed in turn with an aqueous saturated sodium hydrogen carbonate solution, water and saturated saline, dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5→91:9) to obtain the titled compound having the following physical properties (70 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07728023B2uspto-grants-2010_06