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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887648Generated: October 26, 2026

2,2'-Bipyridine → 1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole

https://huagongshe.com/reaction/1887648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
ReactantSodium CarbonateHCID 10340—
Reactant5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazoleHCID 59394660—
CatalystCupric acetateHCID 8895—
Solvent1,2-DichloroethaneHCID 11—
Product1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazoleHCID 59394790104.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of copper (II) acetate (0.902 g, 4.97 mmol) and 2,2′-bipyridine (0.776 g, 4.97 mmol) in DCE (20 mL) is stirred at 70° C. for 15 min, then transferred to a suspension of cyclopropyl trifluoroborate potassium salt (1.47 g, 9.94 mmol) and 5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole (1 g, 4.97 mmol), and sodium carbonate (1.053 g, 9.94 mmol) in DCE (40 mL). The resulting dark-green mixture is stirred at 70° C. for 24 h. T The reaction mixture is partitioned between EtOAc and 1N HCl. The aqueous layer is extracted with EtOAc. The combined organic layers are washed with brine, dried (Na2SO4) and concentrated. The residue (1.64 g) is purified by ISCO (EtOAc-heptane 0-30%) to provide the desired product (1.25 g) as a colorless oil. MS (ESI) m/z 242.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501756B2
Source datasetuspto-grants-2013_08
ORD IDord-afc1831dd3344f4393cc25fb8b4eaf61
Source noteuspto-grants-2013_08