Sodium Bicarbonate → 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline

HRID 1010594

Reaktionsgleichung

Reaktionsgleichung von HRID 1010594
I[C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[N:12]1[CH2:17][CH2:16][N:15]([CH3:18])[CH2:14][CH2:13]1.BrC1C=NC2C(C=1)=CC=CC=2N1CCN(C)CC1.[Na+].[C:38]1([S:44]([O-])(=[O:46])=[O:45])[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1.C(=O)([O-])O.[Na+]>CN(C)C=O.[Cu]I.CO.ClCCl>[CH3:18][N:15]1[CH2:16][CH2:17][N:12]([C:6]2[CH:7]=[CH:8][CH:9]=[C:10]3[C:5]=2[N:4]=[CH:3][C:2]([S:44]([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)(=[O:46])=[O:45])=[CH:11]3)[CH2:13][CH2:14]1

Komponenten

9

Edukt 4

HCID 516892Sodium BicarbonateHCID 517327Sodium benzenesulfonateHCID 673136243-Bromo-8-(4-methyl-piperazin-1-yl)-quinolineHCID 673137463-Iodo-8-(4-methyl-piperazin-1-yl)-quinoline

Produkt 1

HCID 99291628-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinolineAusbeute 7 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)KatalysatorHCID 887MethanolLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

A 4:1 mixture of 3-iodo-8-(4-methyl-piperazin-1-yl)-quinoline (D2) and 3-bromo-8-(4-methyl-piperazin-1-yl)-quinoline (D1) (1.5 g), phenylsulfonic acid sodium salt, dihydrate (2.52 g, 12.6 mmol) and copper (I) iodide (2.4 g, 12.6 mmol) in N,N-dimethylformamide (25 ml) was stirred in an oil bath at 120° C. for 40 h under argon. To the reaction mixture, cooled to ambient temperature, was added 5% sodium hydrogen carbonate solution (100 ml) and dichloromethane (100 ml) with vigorous shaking. The insoluble material was filtered, washed with dichloromethane (3×20 ml) and discarded. The filtrate and washings were transferred to a separating funnel and the layers separated. The aqueous layer was extracted with dichloromethane (100 ml) and the combined organic extracts were washed with water (100 ml), dried (MgSO4) and concentrated in vacuo to an oil (0.9 g). The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane to afford an orange oil (0.28 g, Rf 0.11, methanol/dichloromethane 1:19). This material was further purified by passage through a strong cation exchange (SCX) column eluting firstly with methanol (fractions discarded) and then with methanol/aqueous ammonia-880 (10:1) to give the title compound (E1) as an orange oil (0.152 g, 0.41 mmol, 7% over two steps);

Aufarbeitung

  1. temperatureTo the reaction mixture, cooled to ambient temperature
  2. filtrationThe insoluble material was filtered
  3. washwashed with dichloromethane (3×20 ml)
  4. customThe filtrate and washings were transferred to a separating funnel
  5. customthe layers separated
  6. extractionThe aqueous layer was extracted with dichloromethane (100 ml)
  7. washthe combined organic extracts were washed with water (100 ml)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated in vacuo to an oil (0.9 g)
  10. customThe oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane
  11. customto afford an orange oil (0.28 g, Rf 0.11, methanol/dichloromethane 1:19)
  12. customThis material was further purified by passage through a strong cation exchange (SCX) column
  13. washeluting firstly with methanol (fractions discarded)

Quellen und Nachweise

ORD-Eintrag
ord-a3f4469ddc0d4b6dbb6324c07f5662b3
Quelldatensatz
uspto-grants-2011_07
Patentnummer
US07977337B2

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