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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714884Generated: November 3, 2026

2-Chloro-5-nitropyridine → HCID 57647141, compound

https://huagongshe.com/reaction/1714884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-[2-(Trifluoromethyl)phenoxy]piperidineHCID 5018790—
SolventDimethylformamideHCID 6228—
ProductHCID 57647141HCID 57647141—

Reaction Conditions

Temperature82.5 °C

Reaction Steps

A mixture of 2-chloro-5-nitropyridine (1.6 g, 6.5 mmol), 4-[2-(trifluoromethyl)phenoxy]piperidine (1.2 g, 7.6 mmol), and DBU (2 mL, 13 mmol) in DMF (25 mL) was heated at 80-85° C. for 2 h. The EtOAc extract was washed three times with water, dried (MgSO4) and concentrated. CombiFlash chromatography (120 g, 20-40% EtOAc in hexanes in 20 min, 70 mL/min, 18 mL/fraction) gave the desired product as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799787B2
Source datasetuspto-grants-2010_09
ORD IDord-d0f67c795a44447c8ed6e9447764c988
Source noteuspto-grants-2010_09