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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623092Generated: November 2, 2026

Triethylamine → HCID 57455387, compound

https://huagongshe.com/reaction/1623092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,4-DiethoxybutylamineHCID 80672—
Reactant4-Chloro-3-nitro-1,5-naphthyridineHCID 13122787—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 57455387HCID 57455387101.8%

Reaction Conditions

Temperature5 °C

Reaction Steps

Triethylamine (3.9 mL, 27.9 mmol, 1.2 eq) was added to a suspension of 4-chloro-3-nitro[1,5]naphthyridine (4.87 g, 23.3 mmol, 1.0 eq) in dichloromethane (100 mL). The resulting solution was cooled to 5° C. and 4,4-diethoxybutylamine (5.36 mL, 27.9 mmol, 1.2 eq) was added dropwise over a period of 5 minutes. The reaction mixture was allowed to stir at ambient temperature for 2 hours and then diluted with saturated aqueous sodium bicarbonate (100 mL). The phases were separated and the aqueous phase was extracted with dichloromethane (2×50 mL). The combined organics were dried over magnesium sulfate, filtered, and then concentrated under reduced pressure to provide 7.93 g of (4,4-diethoxybutyl)(3-nitro[1,5]naphthyridin-4-yl)-amine as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778963B2
Source datasetuspto-grants-2014_07
ORD IDord-3838744ebe5d4318bb66a1b52a165bf2
Source noteuspto-grants-2014_07