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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27083Erstellt: 24. Oktober 2026

Butyric Acid → 5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole

https://huagongshe.com/de/reaction/27083

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyric AcidHCID 264—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktRP 35489HCID 3085171—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrroleHCID 1372862767,8%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

Butyric acid (0.71 g.) is added to a suspension of 6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-5-(piperazin-1-yl)carbonyloxy-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole (2.50 g.) and N,N'-dicyclohexyl-carbodiimide (1.67 g.) in anhydrous methylene chloride (50 cc.) and the mixture is stirred for 1 hour at 20° C. After filtering off the dicyclohexylurea formed, washing with methylene chloride (15 cc.) and evaporating the solvent, the residue obtained (3.8 g.) is washed with boiling ethanol (35 cc.) and then recrystallised from a mixture of acetonitrile (110 cc.) and ethanol (11 cc.). 5-(4-Butyrylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole (1.95 g.), which melts at 248° C., is thus obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04220646
Quelldatensatzuspto-grants-1980_09
ORD IDord-156be8bfd6dc4e69a16089b33f19744f
Quellennotizuspto-grants-1980_09