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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43393Generated: October 25, 2026

1,2-Dichloroethane → 4-[5-({(3S)-4-[(4-Chlorophenyl)sulfonyl]-3-methyl-1-piperazinyl}carbonyl)-2-pyridinyl]morpholine

https://huagongshe.com/reaction/43393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthylmorpholineHCID 7525—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant6-Morpholinonicotinic AcidHCID 2776460—
Reactant(2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methylpiperazine hydrochlorideHCID 67028562—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-[5-({(3S)-4-[(4-Chlorophenyl)sulfonyl]-3-methyl-1-piperazinyl}carbonyl)-2-pyridinyl]morpholineHCID 5916136756%

Reaction Steps

To a suspension of (2S)-1-[(4-chlorophenyl)sulfonyl]-2-methylpiperazine hydrochloride (Description 4) (105 mg, 0.338 mmol), EDC (71.3 mg, 0.372 mmol), HOBT.H2O (56.9 mg, 0.372 mmol) and 6-(4-morpholinyl)-3-pyridinecarboxylic acid (77 mg, 0.372 mmol) in DCM (5 ml) was added N-ethyl morpholine (0.090 mL, 0.710 mmol). The reaction was stirred for 18 h at ambient temperature. To the reaction was added water (3 ml) and the organic layer collected via a hydrophobic frit. The organic layer was reduced in volume to approximately 2 ml then loaded onto a silica SP4 chromatography cartridge. The cartridge was eluted with a gradient from 60% ethyl acetate in iso-hexane to ethyl acetate then ethyl acetate. Fractions containing the desired product were combined and reduced in vacuo to yield the title compound as a white solid (88 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536183B2
Source datasetuspto-grants-2013_09
ORD IDord-7fd85d7d94ec4a5893781fa041069bcc
Source noteuspto-grants-2013_09