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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242117Generated: November 1, 2026

3-Fluorobenzylamine → HCID 86645341, compound

https://huagongshe.com/reaction/242117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzylamineHCID 66853—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86645342HCID 86645342—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86645341HCID 8664534197%

Reaction Steps

A solution of 15.6 g (50.6 mmol) 2-chloro-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid chloride in 1,4-dioxane (85 ml) was added in drops to a solution of 7.6 g (60.8 mmol) 3-fluorobenzylamine and 10.3 ml (60.8 mmol) DIPEA in 1,4-dioxane (87 ml). The RS was subsequently stirred for 60 min at RT. The solution was then diluted with water and EA. The organic phase was separated, washed with a 4N aq. NH4Cl sol. and brine, dried over MgSO4 and concentrated in a vacuum. 19.4 g (48.9 mmol, 97%) 2-chloro-N-(3-fluorobenzyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid amide was obtained as a residue. The raw product was further converted without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653101B2
Source datasetuspto-grants-2014_02
ORD IDord-56dc957626f242cf9447b2cb540df22a
Source noteuspto-grants-2014_02