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HRID 25946Erstellt: 23. Oktober 2026

Pyruvic Acid → 2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone

https://huagongshe.com/de/reaction/25946

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyruvic AcidHCID 1060—
EduktThionyl ChlorideHCID 24386—
EduktSodium BicarbonateHCID 516892—
Edukt2',5-dichloro-3-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromideHCID 21325684—
LösungsmittelBenzeneHCID 241—
LösungsmittelChloroformHCID 6212—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenoneHCID 2132574464,8%

Reaktionsschritte

A solution of pyruvic acid (0.33 g) and thionyl chloride (0.27 g) in chloroform (2 ml) is refluxed for 1 hour. After cooling, the solution is mixed with 2',5-dichloro-3-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromide (1.31 g), benzene (6 ml) and dimethylformamide (11 ml) at 0° C. The resultant mixture is stirred at room temperature for 3 hours and allowed to stand overnight. The reaction mixture is neutralized with aqueous sodium bicarbonate and shaken with ethyl acetate. The organic layer is washed with water, dried and evaporated to remove the solvent. The residue is recrystallized from ethyl acetate to give 2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone (0.7 g) as crystals melting at 178° to 180° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147700
Quelldatensatzuspto-grants-1979_04
ORD IDord-9ffa1233d3a54301a7b399e8045faf43
Quellennotizuspto-grants-1979_04