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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1106112Erstellt: 27. Oktober 2026

Chlorotrimethylsilane → HCID 178474807, Verbindung

https://huagongshe.com/reaction/1106112

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
Edukt4-MethylmorpholineHCID 7972—
EduktTriethylamineHCID 8471—
EduktIsobutyl chloroformateHCID 62365—
EduktN-Acetyl-beta-alanineHCID 76406—
EduktHCID 178507442HCID 178507442—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178474807HCID 17847480796,3%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

A solution of 4.6 g (35 mmol) of N-acetyl-beta-alanine, 100 ml acetonitrile, and 3.9 ml (35 mmol) of N-methylmorpholine is stirred at -15° C. and 5.0 ml (38.5 mmol) of isobutyl chloroformate is added. After 30 minutes at -15° C. a solution prepared from 4.05 g (17.5 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid, 7.35 ml (52.5 mmol) of triethylamine, and 7.96 ml (62.7 mmol) of trimethylsilyl chloride in 100 ml of dichloromethane is added and the mixture stirred at -10° C. for 1 hour and at room temperature overnight. The mixture is evaporated to near dryness in vacuo and treated with 200 ml of water. The product is precipitated by acidifying to pH 2.0 and is filtered, washed with water, isopropanol, ether, and dried to give 5.8 g of 2-[4-(N-acetyl-beta-alanylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04311699
Quelldatensatzuspto-grants-1982_01
ORD IDord-2899a12b1d5040b5941ba4b0bcb1bad2
Quellennotizuspto-grants-1982_01