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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376330Generated: October 30, 2026

1-(2-Pyridyl)piperazine → HCID 18704982, compound

https://huagongshe.com/reaction/376330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantHCID 178503844HCID 178503844—
SolventDichloromethaneHCID 6344—
ProductHCID 18704982HCID 1870498295.2%

Reaction Steps

To a mixture of 1-(2-pyridyl)piperazine (10 ml, 64.37 mmol) in dichloromethane (200 ml) was added N-benzoyidimethyldithioimidocarbonate (14.64 g, 65.01 mmol) and the reaction mixture was stirred for 18 h at room temperature. The volatiles were evaporated in vacuo and the residue crystallised from a mixture of heptane/diethyl ether 9:1. The solid was filtered off, washed with a mixture of heptaneldiethyl ether 1:1 and dried in vacuo affording 20.86 g of N-[methylsulfanyl-(4-(pyridin-2-yl)piperazin-1-yl)methylene]-benzamide as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020349
Source datasetuspto-grants-2000_02
ORD IDord-49146d73c98e45ffa2ea80264901f0fa
Source noteuspto-grants-2000_02