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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5793Generated: October 26, 2026

Piperazine → 2-Tert-butyl-5-(4-methyl-piperidin-1-yl)-6-[(piperazin-1-yl)thiocarbonylamino]benzothiazole

https://huagongshe.com/reaction/5793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 15610362—
SolventChloroformHCID 6212—
Product2-Tert-butyl-5-(4-methyl-piperidin-1-yl)-6-[(piperazin-1-yl)thiocarbonylamino]benzothiazoleHCID 5437459369.6%

Reaction Steps

A solution of 3.45 g of 2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole, described in Example 1, and 8.6 g of anhydrous piperazine in 30 ml of chloroform is stirred for 3 hours, washed with water, dried over anhydrous sodium sulphate and evaporated to get a sticky residue which is triturated with isopropanol and filtered to obtain 3 g of 2-tert-butyl-5-(4-methyl-piperidin-1-yl)-6-[(piperazin-1-yl)thiocarbonylamino]benzothiazole, melting at 278°-281°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246927
Source datasetuspto-grants-1993_09
ORD IDord-0021d0cc1d434e90be2099cbc1a36c49
Source noteuspto-grants-1993_09