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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5785Generated: October 26, 2026

Water → 2-Tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazole

https://huagongshe.com/reaction/5785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-MethylpiperidineHCID 69381—
Reactant2-Tert-butyl-5-chloro-6-nitrobenzothiazoleHCID 19794202—
SolventDimethyl SulfoxideHCID 679—
SolventChloroformHCID 6212—
Product2-Tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazoleHCID 19794189—

Reaction Steps

A solution of 32,4 g of 2-tert-butyl-5-chloro-6-nitrobenzothiazole, (described in European patent application 85810418.5 published under No. 0175650) in 300 ml of dimethylsulphoxide, is stirred and heated at 140° for 6 hours with 12.8 g of 4-methylpiperidine and 35.8 g of anhydrous potassium carbonate, cooled and poured into water. The solid obtained is dissolved in chloroform and filtered through a silical gel column. The filtate is evaporated to give 2-tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazole melting at 116°-120°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246927
Source datasetuspto-grants-1993_09
ORD IDord-269df9c1e534472b9cb72738c8208fee
Source noteuspto-grants-1993_09