Phosphorus pentachloride → HCID 10857636, compound

(1)A solution of carbobenzoxy-L-alanine (4.48 g) in tetrahydrofuran (15 ml) is mixed with phosphorus pentachloride (4.58 g) to give a solution of carbobenzoxy-L-alanyl chloride in tetrahydrofuran, which is added to a solution of 1-(2-benzoyl-4-chlorophenyl)-2-(1-amino-1-dimethylcarbamoylmethylene)hydrazine (3.45 g) in tetrahydrofuran (70 ml) and dimethylformamide (20 ml). The resultant mixture is stirred at room temperature for 1 hour, mixed with potassium carbonate (1.38 g), stirred for 4 hours, and allowed to stand overnight. The reaction mixture is mixed with water and evaporated under reduced pressure to remove the solvents, and the residue is extracted with ethyl acetate. The organic layer is dried and evaporated to remove the ethyl acetate, whereby 1-(2-benzoyl-4-chlorophenyl-2-[1-(carbobenzoxy-L-alanylamino)-1-dimethylcarbamoylmethylene]hydrazine is obtained as a residue. The residue is mixed with acetic acid (30 ml) without purification, and the resultant solution is refluxed for 2 hours under heating. The reaction mixture is evaporated under reduced pressure to remove the acetic acid. The residue is extracted with chloroform, and the chloroform layer is washed with aqueous sodium bicarbonate and water in order, dried and evaporated to remove the chloroform. The residue is chromatographed on a column of silica gel, which is eluted with ethyl acetate. The eluate is evaporated to give 5-chloro-2-[3-dimethylcarbamoyl-5-(1-carbobenzoxyaminoethyl)-1H-1,2,4-triazol -1-yl]benzophenone (1.4 g) as a gelatinous material.

ORD record

ord-415548fa5cde4776ad3bf5f9bb75a0eb

Source dataset

uspto-grants-1979_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04159374