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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890543Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 46235653, compound

https://huagongshe.com/reaction/890543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl 3-oxopiperazine-1-carboxylateHCID 736777—
ReactantHCID 22250092HCID 22250092—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 46235653HCID 4623565335.3%

Reaction Conditions

Temperature130 °C

Reaction Steps

To 6-(4-iodophenyl)-1-(4-methoxyphenyl)-3-(methylsulfonyl)-1,4,5,6-tetrahydro-7H-pyrazolo(3,4-c)pyridin-7-one (0.55 g, 1.0 mmol), 4-benzyloxycarbonylpiperazin-2-one (0.35 g, 1.4 mmol), and K2CO3 (0.23 g, 1.6 mmol) was added DMSO (5 mL). The mixture was degassed with N2. CuI (39 mg, 0.21 mmol) was added and the reaction was heated to 130° C. for 18 h. The reaction was diluted with EtOAc and water, extracted with EtOAc, and dried (MgSO4). Purification of the intermediate by chromatography on silica gel using 5% MeOH/CH2Cl2 was followed by deprotection in refluxing TFA. Purification by HPLC and freeze-drying afforded 175 mg (27%) of a white solid; High Resolution Mass Spec (M+H)+ for C24H26N6O5S 496.1650.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995172B2
Source datasetuspto-grants-2006_02
ORD IDord-e5dcd82c72da42778af679887db27cbf
Source noteuspto-grants-2006_02