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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535442Erstellt: 24. Oktober 2026

Triethylamine → Methyl 2-({[2-(dimethylamino)-2-oxoethyl]carbamoyl}amino)-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate

https://huagongshe.com/de/reaction/535442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTriphosgeneHCID 94429—
Edukt2-Amino-N,N-dimethylacetamide acetateHCID 53399009—
EduktMethyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoateHCID 66653263—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktMethyl 2-({[2-(dimethylamino)-2-oxoethyl]carbamoyl}amino)-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoateHCID 66652958143,4%

Reaktionsschritte

0.798 g (2.69 mmol) of triphosgene diluted in 10 ml of dioxane is added, under an inert atmosphere at ambient temperature, to 1.3 g (3.84 mmol) of methyl 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate in 50 ml of dioxane. After stirring for 1 hour, 1.25 g (7.68 mmol) of N,N-dimethylglycinamide acetate and 2.68 ml (19.21 mmol) of triethylamine are added. The reaction medium is stirred overnight at ambient temperature and then hydrolysed with water. The aqueous phase is extracted with dichloromethane. The organic phase obtained is dried over sodium sulphate, filtered, and then concentrated under reduced pressure. 1.8 g of a yellow solid are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859544B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-7fe39e2e149f470199cb02595e447c39
Quellennotizuspto-grants-2014_10