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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718052Generated: October 26, 2026

Pyridine → Methyl 4-(2-(4-fluoro-2-methoxyphenoxy)phenylcarbamoyl)benzoate

https://huagongshe.com/reaction/718052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl 4-(chlorocarbonyl)benzoateHCID 81850—
Reactant2-(4-Fluoro-2-methoxyphenoxy)anilineHCID 59783799—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
ProductMethyl 4-(2-(4-fluoro-2-methoxyphenoxy)phenylcarbamoyl)benzoateHCID 5978373994.1%

Reaction Steps

To a slurry of title compound 91 (4 g, 17.15 mmol) and methyl 4-(chlorocarbonyl)benzoate (3.58 g, 18.01 mmol) in benzene (60 mL) at 0° C. was added pyridine (4.85 mL, 60.0 mmol) drop wise followed by a single crystal of DMAP. The temperature was raised to room temperature and the reaction mixture was left to stir for 1 h. The reaction mixture was filtered and the filtrate was diluted with 5% aq HCl and ethyl acetate. The organic layer was washed with 5% aq HCl, water and brine then left in the fridge over the weekend. The precipitated solid was filtered, washed with water and hexanes to afford title compound 92 (6.38 g, 94%) as an off-white solid. LRMS (ESI): (calc) 395.12. (found) 396.4 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193749B2
Source datasetuspto-grants-2015_11
ORD IDord-9879c2b29fa345bf8d332a212e22f2e5
Source noteuspto-grants-2015_11