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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372120Generated: November 2, 2026

Dimethylformamide → 2-(2-[4-(4-Chloro-phenyl)-piperazin-1-yl]-2-oxo-ethyl)-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1372120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Chloroacetyl)-4-(4-chlorophenyl)piperazineHCID 4053957—
ReactantHCID 178468642HCID 178468642—
SolventEthyl acetate hexaneHCID 21226206—
Product2-(2-[4-(4-Chloro-phenyl)-piperazin-1-yl]-2-oxo-ethyl)-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl esterHCID 58778044—

Reaction Steps

Protocol T was followed using 5-Thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester, K2CO3, 2-Chloro-1-[4-(4-Chloro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=1.5/1) afforded the title compound. 1H NMR (400 MHz, CDCl3): 7.34–7.38 (m, 1H), 7.24–7.26 (m, 1H), 7.12 (s, 1H), 7.04–7.08 (dd, 1H), 6.96–7.2 (m, 2H), 6.88–6.94 (m, 2H), 4.32–4.42 (q, 2H), 3.52–3.58 (m, 4H), 3.05–3.35 (m, 4H), 1.32–1.42 (m, 3H). 13C NMR (400 MHz, CDCl3): 164.2, 128, 126.8, 126.6, 120.2, 118.4, 115.2, 62.5, 54.2, 50.5, 42.6,44, 14.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157464B2
Source datasetuspto-grants-2007_01
ORD IDord-0ed906cdb03449f3bba84c4de5034f70
Source noteuspto-grants-2007_01