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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1589570Erstellt: 26. Oktober 2026

Iodoethane → 1-Ethyl-7-(5-ethyl-2,5-diazabicyclo[2.2.2]-oct-2-yl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, hydroiodide

https://huagongshe.com/reaction/1589570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktTriethylamineHCID 8471—
Edukt7-(2,5-Diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acidHCID 13565797—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Ethyl-7-(5-ethyl-2,5-diazabicyclo[2.2.2]-oct-2-yl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, hydroiodideHCID 13171452357,7%

Reaktionsschritte

A solution of 0.35 g (1.0 mmole) of 7-(2,5-diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, 0.32 ml (4.0 mmole) of ethyl iodide, 0.56 ml (4.0 mmole) triethylamine and 10 ml of N, N-dimethylformamide was heated at 100° for 17 hours. The reaction mixture was evaporated to dryness and the residue was stirred with 25 ml of 1 N sodium hydroxide for one hour. The solution was neutralized to pH 7 with 1 N hydrochloric acid, filtered and evaporated the filtrate to dryness. The residue was recrystallized from ethanol to give 0.29 g of the title compound, mp>300°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04571396
Quelldatensatzuspto-grants-1986_02
ORD IDord-dee1b1e77f69402284755a2f421b158e
Quellennotizuspto-grants-1986_02