Reaktion #57787

ord-435f973cdb9d4431b3d43eeefb9a3641

Reaktionsgleichung

[Cl-].[NH4+]
NH4Cl
Nc1ccc(Cl)cc1C(=O)O
2-amino-5-chlorobenzoic acid
[Li][CH2]CCC
nBuLi
Cn1ccnc1
N-methyl imidazole
Cn1ccnc1C(=O)c1cc(Cl)ccc1N
product
Ausbeute 13.7%
Cn1ccnc1C(=O)c1cc(Cl)ccc1N
(2-Amino-5-chloro-phenyl)-(1-methyl-1H-imidazol-2-yl)-methanone
Ausbeute 13.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturrefluxed for 1 h
  2. 2
    workup.STIRRINGThe reaction mixture was stirred overnight at rt
  3. 3
    Extraktionthe resulting mixture extracted with ethyl acetate (2×150 ml)
  4. 4
    TrocknenThe combined organic layers were dried over Na2SO4
  5. 5
    SonstigeAfter removal of solvent
  6. 6
    Sonstigethe residue was purified by the flash chromatography
  7. 7
    SonstigeCrystallization of the product from Et2O/hexane mixture

Vorschrift

To a solution of nBuLi (0.0730 mol) in hexane was added N-methyl imidazole (0.0608 mol) drop wise at -40° C. over 30 min under a nitrogen atmosphere. The resulting yellow solution was stirred for a further 3 hr at rt, and then refluxed for 1 h. 2-amino-5-chlorobenzoic acid (1.74 g, 0.01014 mole) in dry ether (60 ml) was then added to the reaction mixture. The reaction mixture was stirred overnight at rt. To the reaction mixture was added saturated NH4Cl solution and the resulting mixture extracted with ethyl acetate (2×150 ml). The combined organic layers were dried over Na2SO4. After removal of solvent, the residue was purified by the flash chromatography using ethyl acetate/hexane (1:4) as eluent. Crystallization of the product from Et2O/hexane mixture gave 300 mg (13.7%) of product as yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07420055B2uspto-grants-2008_09