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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1106115Erstellt: 25. Oktober 2026

acetyl-DL-leucine → HCID 178474741, Verbindung

https://huagongshe.com/reaction/1106115

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktacetyl-DL-leucineHCID 1995—
EduktIsobutyl chloroformateHCID 62365—
EduktHCID 178507442HCID 178507442—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktHCID 178474741HCID 17847474171,4%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

A solution of 13.0 g (75 mmol) of N-acetyl-DL-leucine, 10.5 ml (75 mmol) of triethylamine, and 150 ml of dichloromethane is stirred at -10° and 9.75 ml (75 mmol) of isobutyl chloroformate is added. The reaction mixture is stirred for 1/2 hour at -10° C. and a cold solution of 11.6 g (50 mmol) of 2-[4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid and 7.7 (55 mmol) of triethylamine in 200 ml of dimethylformamide is added. The mixture is stirred at 5° C. for 3 hrs and overnight at room temperature. The reaction mixture is evaporated and the residue treated with water. The pH is lowered to 2.5 with dilute hydrochloric acid and the solid filtered, washed with water, and dried to give 13.8 g of 2-[4-(N-acetyl-DL-leucylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid; mp 233°-235° C. dec.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04311699
Quelldatensatzuspto-grants-1982_01
ORD IDord-fceb47acaddf4b658971068ab3942754
Quellennotizuspto-grants-1982_01