Reaktion #1784452

Reaktionsgleichung

diisopropylethylamine

O-(benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate

6-(3,5-dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acid

benzylamine

diisopropylethylamine

→

6-(3,5-dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acid-benzylamide

Lösungsmittel

water

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture is stirred for a further two hours at ambient temperature
2. 2
   Extraktionextracted with ethyl acetate
3. 3
   WaschenThe combined organic extracts are washed with 1N hydrochloric acid, 1N sodium hydroxide solution and saturated sodium chloride solution
4. 4
   Sonstigedried on magnesium sulphate
5. 5
   Sonstigeevaporated down
6. 6
   workup.STIRRINGThe foam-like flask residue is stirred overnight with cyclohexane/ethyl acetate
7. 7
   Filtrationfiltered
8. 8
   Waschenwashed with cyclohexane
9. 9
   Sonstigedried

Vorschrift

1.50 ml diisopropylethylamine and 2.81 g O-(benzotriazol-1-yl)-1,1,3,3-tetramethyluronium-tetrafluoroborate are added to 3.47 g 6-(3,5-dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acid in 15 ml N,N-dimethylformamide. The reaction mixture is stirred for 15 minutes at ambient temperature, then 0.97 ml benzylamine and 1.50 ml diisopropylethylamine are added and the mixture is stirred for a further two hours at ambient temperature. For working up the reaction mixture is mixed with water and extracted with ethyl acetate. The combined organic extracts are washed with 1N hydrochloric acid, 1N sodium hydroxide solution and saturated sodium chloride solution, dried on magnesium sulphate and evaporated down. The foam-like flask residue is stirred overnight with cyclohexane/ethyl acetate and the resulting crystalline precipitate is suction filtered, washed with cyclohexane and dried.

Quelle