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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106235Generated: November 1, 2026

Piperazine → HCID 20553731, compound

https://huagongshe.com/reaction/1106235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 20553732HCID 20553732—
Solvent1-ButanolHCID 263—
ProductHCID 20553731HCID 2055373194%

Reaction Steps

A solution of 6.4 g of 2-bromo-4-(4-phenylsulfinylbenzyl)thiazole (M. P. Kofler: 102° C.) and 6.5 g of anhydrous piperazine in 200 ml of butanol was refluxed for ten hours. Then, the solvent was evaporated and the thus obtained raw oil was taken off with 200 ml of a N solution of CH3SO3H. The insoluble matter was extracted twice with, each time, 20 ml of ether, then alkalized with K2CO3. The thus salted out oil was extracted twice with, each time, 50 ml of chloroform. The chloroform solution was washed with water, dried and evaporated. There was obtained 6.1 g of 1-[4-(4-phenylsulfinylbenzyl)-2-thiazolyl]piperazine, as semicrystallized product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312869
Source datasetuspto-grants-1982_01
ORD IDord-4f09e925909b4546b3140f5d997f424b
Source noteuspto-grants-1982_01