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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497227Generated: October 26, 2026

Triethylamine → 2-Amino-3-fluoro-N-methoxy-N-methyl-benzamide

https://huagongshe.com/reaction/1497227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant8-Fluoroisatoic anhydrideHCID 10535393—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-3-fluoro-N-methoxy-N-methyl-benzamideHCID 8150749280.4%

Reaction Steps

To a suspension of N,O-dimethylhydroxylamine hydrochloride (703 mg, 7.21 mmol) in ethanol (5.4 ml) and water (0.6 ml) was added triethylamine (729 mg, 1.00 ml, 7.21 mmol) and the mixture was stirred for 10 min at room temperature. Then 8-fluoro-1H-benzo[d][1,3]oxazine-2,4-dione (870 mg, 4.8 mmol) and additional ethanol (2 ml) were added and the reaction mixture was heated to reflux for 3.5 h. After cooling to room temperature, the mixture was poured onto ice/saturated NaHCO3-solution, extracted with EtOAc and the combined extracts were washed with water and brine, dried with Na2SO4 and evaporated. The remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 80:20-70:30) to afford the title compound (765 mg, 80%) as light brown oil. MS (ESI): 199.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199938B2
Source datasetuspto-grants-2015_12
ORD IDord-257c720c80f5445db144cbd6c40acd8b
Source noteuspto-grants-2015_12