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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473699Generated: October 30, 2026

2-Fluoropyridine → HCID 59373935, compound

https://huagongshe.com/reaction/473699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantPhenol, 4-amino-2-fluoro-HCID 2735918—
SolventEthyl AcetateHCID 8857—
ProductHCID 59373935HCID 59373935—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 4-amino-2-fluorophenol (0.983 g, 7.73 mmol) was added NMP (3 mL) and 2-fluoropyridine (0.670 mL, 7.78 mmol). The reaction mixture was heated to 120° C. for 12.5 h and the temperature was increased to 150° C. After 9 h, the reaction mixture was diluted with EtOAc and the organic phase was washed with saturated NaHCO3 (1×), brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (10% to 70% EtOAc in hexanes) gave 2-fluoro-4-(pyridin-2-ylamino)phenol as a pale yellow oil. MS (ESI, pos. ion) m/z: 205.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-16e84d64c15a46a786cd396e4a90acd0
Source noteuspto-grants-2014_01