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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029238Generated: October 25, 2026

N-(4-Aminophenyl)-4-fluoro-2-trifluoromethyl-benzamide → N-(2-(Dimethylamino)ethyl)-1-(4-(4-fluoro-2-(trifluoromethyl)benzamido)phenyl amino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide

https://huagongshe.com/reaction/1029238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Aminophenyl)-4-fluoro-2-trifluoromethyl-benzamideHCID 44603462—
Reactant1-Chloro-N-(2-(dimethylamino)ethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamideHCID 69810673—
ProductN-(2-(Dimethylamino)ethyl)-1-(4-(4-fluoro-2-(trifluoromethyl)benzamido)phenyl amino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamideHCID 4420638950%

Reaction Steps

The title compound was synthesized according to the procedure described for the preparation of Example 267 using 296 (40 mg, 0.12 mmol), and N-(4-aminophenyl)-4-fluoro-2-(trifluoromethyl)benzamide (36 mg, 0.12 mmol) to provide 297 (35 mg, 50% yield) as a solid. LC-MS (M+H=607, obsd.=607).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735584B2
Source datasetuspto-grants-2014_05
ORD IDord-e5d4e2cf153f4565b593f32fa5ddc68e
Source noteuspto-grants-2014_05