Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118750Generated: October 25, 2026

Water → 2-Tert-butyl-6-nitro-5-[4-phenylpiperazin-1-yl]benzothiazole

https://huagongshe.com/reaction/2118750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-PhenylpiperazineHCID 7096—
Reactant2-Tert-butyl-5-chloro-6-nitrobenzothiazoleHCID 19794202—
Product2-Tert-butyl-6-nitro-5-[4-phenylpiperazin-1-yl]benzothiazoleHCID 20192955—

Reaction Steps

A mixture of 7 g of 2-tert-butyl-5-chloro-6-nitrobenzothiazole described in Example 5, in 8.2 g of N-phenylpiperazine is heated at 150°-160° for 12 hours, cooled and poured into water. The paste is extracted with methylene chloride, washed with 2N HCl, then with 10% NaOH and then with water. The organic layer is dried, the solvent evaporated and the solid crystallised from isopropyl alcohol to give 2-tert-butyl-6-nitro-5-[4-phenylpiperazin-1-yl]benzothiazole, melting at 152°-155°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680301
Source datasetuspto-grants-1987_07
ORD IDord-d21f091a14494fe698eebfb69a479ee2
Source noteuspto-grants-1987_07