تفاعل #1053670

ord-9563e1b31876465d9aa7aa24f2088ddd

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    درجة الحرارةto reflux for 18 hours
  3. 3
    أخرىThen the reaction was quenched with saturated sodium bicarbonate
  4. 4
    استخلاصextracted with ethyl acetate (3×)
  5. 5
    غسيلThe combined organic phases were washed with brine
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    أخرىAfter removing the solvent
  8. 8
    أخرىchromatographed
  9. 9
    غسيلeluting with ethyl acetate/methanol/triethyl amine (100/10/1)

الإجراء التجريبي

5-(2-Methanesulfonyloxy-ethyl)-2-methyl-1H-indole-3-carboxylic acid benzyl ester (0.350 g, 0.900 mmol, 1 eq, Example 56, Step D) was suspended in dioxane (20 mL) under Ar. (R)-2-(Methoxymethyl)-pyrrolidine (0.207 g, 1.800 mmol, 2 eq) was added. The reaction mixture was stirred and heated to reflux for 18 hours. Then the reaction was quenched with saturated sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic phases were washed with brine and dried over Na2SO4. After removing the solvent, the residue was loaded on silica gel and chromatographed, eluting with ethyl acetate/methanol/triethyl amine (100/10/1). 0.300 g (82%) of the indole-amine was obtained as a white solid. This was converted to the .HCl salt. LC/MS (ESI+) 407 (M+1); Anal. Calcd for C25H30N2O3.1 HCl.1H2O: C, 65.14; H, 7.22; N, 6.08; Found: C, 65.07; H, 7.08; N, 6.19.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06951848B2uspto-grants-2005_10