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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185263Generated: October 25, 2026

Diisopropylethylamine → 3,3-difluoro-1-(1-methyl-4-nitro-1H-pyrazol-5-yl)piperidine

https://huagongshe.com/reaction/1185263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,3-Difluoropiperidine hydrochlorideHCID 2758349—
Reactant5-chloro-1-methyl-4-nitro-1H-pyrazoleHCID 12344836—
SolventEthanolHCID 702—
Product3,3-difluoro-1-(1-methyl-4-nitro-1H-pyrazol-5-yl)piperidineHCID 5846497883%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 5-chloro-1-methyl-4-nitro-1H-pyrazole (0.1 g, 4.5 mmol), 3,3-difluoropiperidine hydrochloride (0.14 g, 0.93 mmol) and DIPEA (0.5 mL, 2.8 mmol) in EtOH (3 mL) was heated at 130° C. in a microwave for 1 hr. Additional DIPEA (0.5 mL, 2.8 mmol) and 3,3-difluoropiperidine hydrochloride (0.29 g, 1.8 mmol) were added and the mixture was heated at 130° C. in a microwave for 2 hr. The solvent was removed under reduced pressure and the crude product was purified via silica gel column chromatography (0-60% EtOAc/isohexane) to yield 3,3-difluoro-1-(1-methyl-4-nitro-1H-pyrazol-5-yl)piperidine as a yellow oil (127 mg, 83%). 1H NMR (400 MHz, CDCl3) δ 8.04 (s, 1H), 3.80 (s, 3H), 3.41-3.29 (m, 2H), 3.26-3.04 (m, 2H), 2.17-2.03 (m, 2H), 1.97-1.88 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669361B2
Source datasetuspto-grants-2014_03
ORD IDord-ba48f46289694f70b121587778e60d02
Source noteuspto-grants-2014_03