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HRID 67454Erstellt: 25. Oktober 2026

Hydrochloric Acid → (2,4-Dimethoxy-benzylamino)-acetic acid

https://huagongshe.com/reaction/67454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktGlycineHCID 750—
EduktSodium ChlorideHCID 5234—
EduktIsatoic AnhydrideHCID 8359—
EduktSodium HydroxideHCID 14798—
Edukt2,4-DimethoxybenzaldehydeHCID 69175—
Edukt(2,4-Dimethoxy-benzylamino)-acetic acidHCID 11042399—
KatalysatorPalladiumHCID 23938—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt(2,4-Dimethoxy-benzylamino)-acetic acidHCID 11042399—
Produkt3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dioneHCID 21764314—

Reaktionsschritte

N-(2,4-dimethoxybenzyl)glycine is prepared by the reaction of glycine with 2,4-dimethoxybenzaldehyde in the presence of sodium hydroxide, reduction with palladium-on-carbon in methanol and subsequent neutralisation with 2 N hydrochloric acid. The aqueous solution obtained is concentrated. 41.9 g of this mixture of N-(2,4-dimethoxybenzyl)-glycine and sodium chloride are stirred at 110° C. for 1.5 hours in 300 ml of dimethyl sulphoxide with 23.18 g (142 mmol) of isatoic acid anhydride. The mixture is poured into ca 2 liters of water and stirred for 0.5 hour. The separated crystals are filtered off under suction, washed with water and dried. After recrystallisation from ethyl acetate, there is obtained 3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dione of melting point 151°-152.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04346034
Quelldatensatzuspto-grants-1982_08
ORD IDord-84b7bb43a85845de858776ebd3ea7b8e
Quellennotizuspto-grants-1982_08