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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414736Generated: October 29, 2026

Nitrogen → HCID 19865441, compound

https://huagongshe.com/reaction/414736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiethylcarbamoyl chlorideHCID 6916—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 54680203HCID 54680203—
SolventAcetic AcidHCID 176—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 19865441HCID 19865441—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-(1,2-dihydro-4-hydroxy-1-phenyl-2-oxo-1,8-naphthyridin-3-yl)-pyrrolidinium hydroxide, inner salt (3 g), triethylamine (1.88 g), and diethylcarbamoyl chloride (1.57 g) in dry pyridine (50 mL) was stirred overnight at room temperature in an N2 atmosphere. Some starting material remained so dimethylformamide (50 mL), 1,8-diazabicyclo[5.4.0]undec7-ene (DBU) (2.83 g), and diethylcarbamoyl chloride (1.57 g) were added and the mixture was heated at 80° C. for 0.5 hour. The reaction mixture was then poured over ice and the pH was adjusted to about 6 with acetic acid. The resulting solution was extracted three times with ethyl acetate. The organic extracts were combined, dried (Na2SO4), filtered and evaporated to a solid which was recrystallized from isopropanol to yield the desired product, 2.03 g (54%), m.p. 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04794116
Source datasetuspto-grants-1988_12
ORD IDord-90bdb6d1793844498e0de311b6f82ca0
Source noteuspto-grants-1988_12