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Pyrrolidine → 5-(4-Methylpiperazin-1-yl)-1H-indole

HRID 1406416
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1406416
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[C:10]([CH3:17])[CH:9]=2)[CH2:4][CH2:3]1.[CH3:18]OC(OC)N(C)C.N1CCCC1.C([O-])=O.[NH4+]>CN(C)C=O.[Pd]>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:9]=[C:10]3[C:11](=[CH:12][CH:13]=2)[NH:14][CH:18]=[CH:17]3)[CH2:4][CH2:3]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 31268PyrrolidineHCID 78373Dimethylformamide dimethyl acetalHCID 2723923Ammonium formateHCID 184397471-Methyl-4-(3-methyl-4-nitrophenyl)piperazine

Produkt 1

HCID 220154055-(4-Methylpiperazin-1-yl)-1H-indole

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938
Palladium
Katalysator
HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A solution of 1-methyl-4-(3-methyl-4-nitro-phenyl)-piperazine (10a), (2.63 g, 11.2 mmol), N,N-dimethylformamide dimethyl acetal (4.7 mL, 35.84 mmol) and pyrrolidine (1.5 mL, 17.9 mmol) in anhydrous N,N-dimethylformamide (20 mL) was heated at 120° C. for 18 hours. The reaction mixture was concentrated in vacuo, taken up in ethanol (50 mL) containing 2 mL of water and to this was added ammonium formate (3.67 g, 58.2 mmol). Palladium, 10 wt. % on activated carbon (0.84 g) was added and the suspension was stirred and heated at 50° C. for 30 minutes. The reaction mixture was then filtered through a celite pad and the pad rinsed with hot methanol (20 mL). The combined filtrate and washings were concentrated in vacuo and the residue was taken up in ethyl acetate (100 mL), washed with aqueous saturated sodium bicarbonate solution (2×100 mL), brine, dried (MgSO4) and concentrated in vacuo. The resultant crude product was purified by flash chromatography on SiO2 eluting first with hexane and then 15% ethyl acetate/hexane to afford the desired title compound as an off-white solid, 1.44 g, 60%.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. additioncontaining 2 mL of water
  3. filtrationThe reaction mixture was then filtered through a celite pad
  4. washthe pad rinsed with hot methanol (20 mL)
  5. concentrationThe combined filtrate and washings were concentrated in vacuo
  6. washwashed with aqueous saturated sodium bicarbonate solution (2×100 mL), brine
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo
  9. customThe resultant crude product was purified by flash chromatography on SiO2 eluting first with hexane

Quellen und Nachweise

ORD-Eintrag
ord-60487c174c3240e9aed9569e1186def4
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08916591B2

Notizen zur Reaktion

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