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(R)-5-(2-Ethylsulphonylethenyl)-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole → (R)-5-(2-Ethylsulphonylethyl)-3-(N-methylpyrrolidin-2-ylmethyl)1H-indole

HRID 744151
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인쇄 미리보기

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HRID 744151 반응식
[CH2:1]([S:3]([CH:6]=[CH:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[C:11]2[CH2:17][C@H:18]1[CH2:22][CH2:21][CH2:20][N:19]1[CH3:23])(=[O:5])=[O:4])[CH3:2]>Cl.CN(C)C=O.O.[Pd]>[CH2:1]([S:3]([CH2:6][CH2:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[C:11]2[CH2:17][C@H:18]1[CH2:22][CH2:21][CH2:20][N:19]1[CH3:23])(=[O:5])=[O:4])[CH3:2]
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참가 물질

6

반응물 1

HCID 54504320(R)-5-(2-Ethylsulphonylethenyl)-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole

생성물 1

HCID 9884122(R)-5-(2-Ethylsulphonylethyl)-3-(N-methylpyrrolidin-2-ylmethyl)1H-indole수율 69.6%

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 313Hydrochloric Acid용매HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

(R)-5-(2 -Ethylsulphonylethenyl)-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole (157 mg) was dissolved in a mixture of ethanolic hydrogen chloride [prepared by addition of acetyl chloride (0,043 mL) to ethanol (10 mL)], N,N-dimethylformamide (7.5 mL) and water (0.1 mL) and the solution was shaken under a hydrogen atmosphere (15 psi) at room temperature for 18 hours in the presence of 10% palladium on carbon (150 mg). The mixture was filtered through Arbacel (trade mark) filter aid and the residue was washed well with ethanol. The combined filtrate and washings were evaporated under reduced pressure and the residual oil was partitioned between ethyl acetate and 2M aqueous sodium carbonate solution. The organic layer was separated, washed three times with water followed by brine and then dried (Na2SO4). Evaporation of the solvent gave an oil which was chromatographed on silica gel. Elution with dichloromethane/methanol/concentrated aqueous ammonia (90:10:1) gave the title compound as a gum (110 mg): TLC (CH2Cl2 /C2H5OH/NH3 ; 90:10:1): Rf =0.3; [α]25D =+62° (methanol, c=0.10). Anal. Calcd for C18H26N2O2S. 0.05 CH2Cl2 : C,63.21; H,7.67; N,8.17. Found: C,63.55; H,7.61; N,8.41.

후처리

  1. filtrationThe mixture was filtered through Arbacel (trade mark)
  2. filtrationfilter aid
  3. washthe residue was washed well with ethanol
  4. customThe combined filtrate and washings were evaporated under reduced pressure
  5. customthe residual oil was partitioned between ethyl acetate and 2M aqueous sodium carbonate solution
  6. customThe organic layer was separated
  7. washwashed three times with water
  8. dry with materialdried (Na2SO4)
  9. customEvaporation of the solvent
  10. customgave an oil which
  11. customwas chromatographed on silica gel
  12. washElution with dichloromethane/methanol/concentrated aqueous ammonia (90:10:1)

출처 및 근거

ORD 기록
ord-c31db11156eb4fa2956701a5cff6802b
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05559129

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