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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18933Generated: October 26, 2026

Phosphorus pentachloride → 4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one

https://huagongshe.com/reaction/18933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Piperazinone, 3,3-dimethyl-HCID 211157—
Reactant5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acidHCID 18322391—
SolventDichloromethaneHCID 6344—
Product4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 5867927253.1%

Reaction Steps

The previously prepared 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acid (0.203 g, 1.11 mmol) and PCl5 (0.232 g, 1.11 mmol) were dissolved in dichloromethane (4 mL) and stirred at room temperature for 5 minutes. The resulting solution was added in one portion to a solution of 3,3-dimethylpiperazin-2-one (0.214 g, 1.67 mmol) and DIEA (0.288 g, 2.23 mmol) in dichloromethane (3 mL) and stirred at room temperature for 5 minutes. The reaction mixture was diluted with dichloromethane and washed sequentially with 1N aqueous HCl, saturated sodium bicarbonate, dried and the solvent removed under vacuum. The crude product was purified by chromatographic column (silica gel, dichloromethane:methanol, 95:5) to afford 0.190 g of expected 4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741479B2
Source datasetuspto-grants-2010_06
ORD IDord-322741f3750e433294754e2aba2b83fd
Source noteuspto-grants-2010_06