N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]thiazol-2-yl}acetamide → N-{4-[2-(4-aminophenyl)ethyl]thiazol-2-yl}acetamide

HRID 1246423Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1246423
[N+:1]([C:4]1[CH:9]=[CH:8][C:7](/[CH:10]=[CH:11]\[C:12]2[N:13]=[C:14]([NH:17][C:18](=[O:20])[CH3:19])[S:15][CH:16]=2)=[CH:6][CH:5]=1)([O-])=O.[H][H]>CO.O1CCCC1.C(O)(=O)C.[C].[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][C:12]2[N:13]=[C:14]([NH:17][C:18](=[O:20])[CH3:19])[S:15][CH:16]=2)=[CH:6][CH:5]=1

Komponenten

7

Edukt 2

HCID 58720254N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]thiazol-2-yl}acetamideHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 21914814N-{4-[2-(4-aminophenyl)ethyl]thiazol-2-yl}acetamideAusbeute 29,9 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 178418390HCID 178418390, VerbindungKatalysatorHCID 176Acetic AcidLösungsmittelHCID 887MethanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A mixture of N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]-1,3-thiazol-2-yl}acetamide (2 g) and 10% palladium carbon (400 mg) in methanol (25 ml), tetrahydrofuran (25 ml) and acetic acid (18 ml) was stirred under 4 atm hydrogen at ambient temperature for 5 hours. The reaction mixture was filtered through a celite pad, and the filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate. The organic solution was washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by flash column chromatography over silica gel with n-hexane/ethyl acetate (1:2)→ethyl acetate as an eluent, and triturated with ethyl alcohol/ethyl ether to give N-(4-(2-(4-aminophenyl)ethyl)-1,3-thiazol-2-yl)acetamide (539.6 mg) as an off-white solid.

Aufarbeitung

  1. filtrationThe reaction mixture was filtered through a celite pad
  2. concentrationthe filtrate was concentrated in vacuo
  3. dissolutionThe residue was dissolved in ethyl acetate
  4. washThe organic solution was washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash column chromatography over silica gel with n-hexane/ethyl acetate (1:2)
  8. customtriturated with ethyl alcohol/ethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-bd1fbdfa6ba24800b6c3501fd4463847
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07125901B2

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