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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415617Generated: November 3, 2026

4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline → HCID 178523789, compound

https://huagongshe.com/reaction/2415617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-fluoro-2-(trifluoromethyl)quinolineHCID 2736591—
ReactantN-(4-aminocyclohexyl)-3,5-difluorobenzamideHCID 22641525—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178523789HCID 178523789—

Reaction Steps

A solution of N-(4-Amino-cyclohexyl)-3,5-difluorobenzamide (30 mg, 0.12 mmol) in NMP (1.0 mL) was treated with 4-chloro-6-fluoro-2-trifluoromethyl-quinoline (1 eq) and 3 eq (0.045 mL) TEA. The reaction was heated to 220 C in the microwave for 15 minutes. The crude compound was purified by reverse phase HPLC to provide the desired compound. MS (ESI (+)) m/e 468 (M+H)+; 1H NMR (500 MHz, DMSO) δ ppm 8.32 (m, 2 H), 7.98 (m, 1 H), 7.67 (m, 1 H), 7.58 (m, 2 H), 7.44 (m, 1 H), 7.15 (d, 1 H), 6.82 (s, 1 H), 1.95 (m, 4 H), 1.65-1.88 (m, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818772B2
Source datasetuspto-grants-2004_11
ORD IDord-4787ccb1b4b842df84cd8b6cab01970f
Source noteuspto-grants-2004_11