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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201567Generated: October 28, 2026

2-Fluoroaniline → HCID 117771064, compound

https://huagongshe.com/reaction/2201567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Amino-6-bromopicolinic acidHCID 45480452—
SolventTolueneHCID 1140—
ProductHCID 117771064HCID 11777106445%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-amino-6-bromopicolinic acid (250 mg, 1.152 mmol) and SOCl2 (5 mL) in toluene (10 mL) was stirred at 130° C. for 2 h, then evaporated and dissolved in tetrahydrofuran (20 mL). 2-fluoro-phenylamine (256 mg, 2.3 mmol) was added dropwise maintaining the temperature at 5° C. The reaction mixture was heated to 90° C. for 15 h. The mixture was cooled to room temperature and quenched with saturated aqueous K2CO3 (10 mL) and extracted with ethyl acetate (10 mL*3), the combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified with column chromatograph (PE:EtOAc=3:1) to give 3-amino-6-bromo-N-(2-fluorophenyl)picolinamide (160 mg, yield: 45%). MS (M+H)+: 311/313.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-993ad29fe5624e4bab27df1bdf77d34e
Source noteuspto-grants-2016_06