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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4,4-Difluoropiperidine hydrochloride | HCID 2758351 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67237449 | HCID 67237449 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08691938B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-e8a9e857cc9a4e8bbfbf14280c908f13 |
|---|
| Source note | uspto-grants-2014_04 |
|---|