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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1106114Erstellt: 26. Oktober 2026

N-Acetyl-DL-methionine → HCID 178503723, Verbindung

https://huagongshe.com/reaction/1106114

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Acetyl-DL-methionineHCID 6180—
EduktDimethylacetamideHCID 31374—
EduktIsobutyl chloroformateHCID 62365—
EduktHCID 178507442HCID 178507442—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktHCID 178503723HCID 17850372357,1%

Reaktionsschritte

A suspension of 14.34 g (75 mmol) of N-acetyl-DL-methionine and 150 ml of dichloromethane is stirred at -15° and 10.5 ml (75 mmol) of triethylamine is added followed by 9.75 ml (75 mmol) of isobutyl chloroformate. After stirring for 20 minutes at -15° C., a solution of 11.6 g (50 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid in 200 ml of dimethylacetamide containing 7.7 ml (55 mmol) of triethylamine is added at -15° C. The mixture is stirred at 0° C. for 3 hrs and overnight at room temperature. The mixture is evaporated and the residue triturated with water. The aqueous suspension, after adjusting the pH to 2.5 with dilute HCl is filtered, washed with water, and dried to give 11.54 g of 2-[4-(N-acetyl-DL-methionylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid; mp 259° C. dec.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04311699
Quelldatensatzuspto-grants-1982_01
ORD IDord-05d69929a85042e98f25dfbd14c9cd8c
Quellennotizuspto-grants-1982_01