Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521343Generated: October 25, 2026

Methyl 3-amino-4-fluorobenzoate → 3-Amino-N-(2-(2,6-cis-dimethylpiperidin-1-yl)ethyl)-4-fluorobenzamide

https://huagongshe.com/reaction/1521343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-amino-4-fluorobenzoateHCID 12541234—
Reactant2-(2,6-cis-Dimethylpiperidin-1-yl)ethanaminium chlorideHCID 86695686—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-N-(2-(2,6-cis-dimethylpiperidin-1-yl)ethyl)-4-fluorobenzamideHCID 86695685—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture comprising 2-(2,6-cis-dimethylpiperidin-1-yl)ethanaminium chloride (4 g, 20.75 mmol) and methyl 3-amino-4-fluorobenzoate (3.51 g, 20.75 mmol) in THF (50 ml) was treated with TBD (2.89 g, 20.75 mmol) and stirred at 80° C. for 16 hrs. A further portion of methyl 3-amino-4-fluoro benzoate (1 g) and TBD (0.5 g) were added and heating continued for 24 hrs. The resulting mixture was partitioned between ethyl acetate and aqueous sodium bicarbonate. The mixture was extracted once with ethyl acetate and once with chloroform. The combined organic layers were dried (MgSO4), filtered and evaporated to dryness. Purification of the residue by chromatography on silica eluting with 0-20% MeOH in DCM afforded the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073921B2
Source datasetuspto-grants-2015_07
ORD IDord-ad35993110bd4bea81ffe90a95e1a147
Source noteuspto-grants-2015_07