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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364849Generated: October 29, 2026

2-Chloro-5-nitropyridine → HCID 67237449, compound

https://huagongshe.com/reaction/2364849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4-Difluoropiperidine hydrochlorideHCID 2758351—
SolventEthanolHCID 702—
ProductHCID 67237449HCID 67237449—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a slurry of 2-chloro-5-nitropyridine (5 g, 31.5 mmol) and 4,4-difluoropiperidine hydrochloride (4.97 g) in ethanol (40 mL) at ambient temperature was added N,N-diisopropylethylamine (12.00 mL, 69.4 mmol) and the mixture heated to 70° C. for 18 hours. The reaction was concentrated, partitioned between CH2Cl2 and 1M NaOH. The organic phase concentrated and purified by chromatography (elution with 2% MeOH—CH2Cl2 then 3% MeOH—CH2Cl2) to provide the title compound as a yellow oil. MS (DCI) m/z 261 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691938B2
Source datasetuspto-grants-2014_04
ORD IDord-e8a9e857cc9a4e8bbfbf14280c908f13
Source noteuspto-grants-2014_04