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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(3-Trifluoromethylphenyl)piperidine, HCl | HCID 22252849 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5'-nitro-4-(3-triflouromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl | HCID 67435710 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211914B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-e7cd920c181047d0ab99ade5893f496e |
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| Source note | uspto-grants-2012_07 |
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