p-Toluidine → N-(4-Methylphenyl)-2-{[(1,1-dimethylethoxy)carbonyl]amino]-6-methylbenzamide

HRID 1814988Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1814988
CN1CCOCC1.[CH3:8][C:9]([CH3:25])([O:11][C:12]([NH:14][C:15]1[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:16]=1[C:17]([OH:19])=O)=[O:13])[CH3:10].[NH2:26][C:27]1[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=1.C(=O)([O-])O.[Na+]>CN(C)C=O>[CH3:33][C:30]1[CH:31]=[CH:32][C:27]([NH:26][C:17](=[O:19])[C:16]2[C:20]([CH3:24])=[CH:21][CH:22]=[CH:23][C:15]=2[NH:14][C:12]([O:11][C:9]([CH3:8])([CH3:10])[CH3:25])=[O:13])=[CH:28][CH:29]=1

Komponenten

6

Edukt 4

HCID 7813p-ToluidineHCID 79724-MethylmorpholineHCID 516892Sodium BicarbonateHCID 222451232-((tert-Butoxycarbonyl)amino)-6-methylbenzoic acid

Produkt 1

HCID 22245130N-(4-Methylphenyl)-2-{[(1,1-dimethylethoxy)carbonyl]amino]-6-methylbenzamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
18 °C

Versuchsvorschrift

Firstly N-methylmorpholine (6.15 mL. 5.64 g, 55.8 mmol) and then O-(benzotriazol-1-yl N,N,N′N′-tetramethyluronium hexalfuorophosphate (10.15 g, 26.8 mmol) are added to a stirred mixture of 2-{([(1,1-dimethylethoxy)carbonyl]amino}-6-methylbenzoic acid (5.60 g, 22.3 mmol) and p-toluidine 4.78 g, 44.6 mmol) in dry dimethylformamide (110 mL) under an argon atmosphere, and stirred at 18° C. for 16 hours. The solvent is evaporated off under reduced pressure to give a residue which is treated with aqueous sodium hydrogen carbonate solution (200 mL of 10%) and extracted with dichloromethane (3×100 mL). The combined extracts are washed with aqueous citric acid solution (100 mL of 10%), dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent 20% ethyl acetate in hexane, and recrystallised from tert-butyl methyl ether-hexane to give the title compound as a colourless crystalline solid, m.p. 250° C.

Aufarbeitung

  1. customThe solvent is evaporated off under reduced pressure
  2. customto give a residue which
  3. extractionextracted with dichloromethane (3×100 mL)
  4. washThe combined extracts are washed with aqueous citric acid solution (100 mL of 10%)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customthe solvent is evaporated off under reduced pressure
  8. customto yield the crude product which
  9. customis purified by column chromatography on silica gel, eluent 20% ethyl acetate in hexane
  10. customrecrystallised from tert-butyl methyl ether-hexane

Quellen und Nachweise

ORD-Eintrag
ord-7b46e7d019d643568bce576ae9494f20
Quelldatensatz
uspto-grants-2005_04
Patentnummer
US06878720B2

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