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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262710Generated: November 3, 2026

Potassium Carbonate → HCID 57443120, compound

https://huagongshe.com/reaction/2262710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,6-DichloropyridazineHCID 67331—
ReactantHCID 57442330HCID 57442330—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57443120HCID 57443120—

Reaction Steps

Dissolve 1-cyclobutyl-4-(piperazin-1-ylacetyl)piperazine (2.05 g, 5.46 mmol) and 3,6-dichloropyridazine (810 mg, 5.46 mmol) in dry DMSO (25 mL). Add K2CO3 (3.77 g, 27.3 mmol) and heat the mixture at 120° C. overnight. Cool and partition between CH2Cl2 (100 mL) and 1 N NaOH (150 mL). Extract the aqueous phase with CH2Cl2 (2×100 mL). Combine, dry and evaporate the organic extracts. Triturate the resulting residue with ether and filter off the solid (product). Evaporate the filtrate and chromatograph the resulting residue with EtOAc followed by EtOAc/MeOH (95:5) and EtOAc/MeOH/TEA(95:5:5) to yield additional product. 1H NMR (CDCl3) δ 7.21 (d, 1H), 6.89 (d, 1H), 3.68-3.59 (m, 8H), 3.22 (s, 2H), 2.78-2.62 (m, 5H), 2.38-2.28 (m, 4H), 2.13-2.03 (m, 2H), 1.93-1.8 (m, 2H), 1.73-1.69 (m, 2H); LC-MS (M+1) 378.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851474B2
Source datasetuspto-grants-2010_12
ORD IDord-6bf5eb30237c41a39ef64abac19e470c
Source noteuspto-grants-2010_12