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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981196Generated: October 31, 2026

Methylamine → 3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine

https://huagongshe.com/reaction/981196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl 2-(2-chloro-6,7,8-trifluoro-3-quinolinecarbonyl)(dimethylamino)acrylateHCID 53994177—
SolventEthanolHCID 702—
Product3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 1942368879.9%

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution, at about 5° C., of 10 g of methylamine in 50 cm3 of ethanol is added in the course of 10 minutes, at between 5° and 10° C., to a stirred suspension of 19.3 g of ethyl 2-(2-chloro-6,7,8-trifluoro-quinoline-3-carbonyl)-3-dimethylaminoacrylate in 150 cm3 of ethanol kept at a temperature close to 5° C., the mixture is stirred for 1 hour at between 5° and 10° C. and the temperature is allowed to rise to about 20° C. 7.6 g of DBU are added to the solution obtained and the mixture is heated at about 30° C. for 1 hour. After cooling to a temperature close to 20° C., the product is drained and washed with twice 100 cm3 of ethanol and twice 100 cm, of diisopropyl ether. 13.4 g of 3-ethoxycarbonyl-7,8,9 -trifluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine are obtained in the form of a yellow solid melting at 320° C., which is used for the subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990515
Source datasetuspto-grants-1991_02
ORD IDord-591c1c57dc6345718f13da893e46feee
Source noteuspto-grants-1991_02