Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510260Generated: October 26, 2026

2-Chloro-5-nitropyridine → 5'-nitro-4-(3-triflouromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl

https://huagongshe.com/reaction/1510260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(3-Trifluoromethylphenyl)piperidine, HClHCID 22252849—
SolventDimethylformamideHCID 6228—
Product5'-nitro-4-(3-triflouromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinylHCID 67435710—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-chloro-5-nitropyridine (500 mg, 3.2 mmol) and 4-(3-trifluoromethyl-phenyl)-piperidine hydrochloride in DMF (15 mL) was added diisopropylethylamine (1.70 mL, 9.60 mmol). The mixture was heated in a sealed tube at 80° C. for 24 hours. The mixture was concentrated to dryness and triturated in methanol to give 5′-nitro-4-(3-triflouromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl. The NMR spectrum obtained on the sample is compatible with its structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211914B2
Source datasetuspto-grants-2012_07
ORD IDord-e7cd920c181047d0ab99ade5893f496e
Source noteuspto-grants-2012_07