Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118761Generated: October 25, 2026

2-Tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazole → 6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole

https://huagongshe.com/reaction/2118761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazoleHCID 19794189—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 19794186—

Reaction Steps

A solution of 15.2 g of 2-tert-butyl-5-[4-methylpiperidin-1-yl]-6-nitrobenzothiazole in 600 ml of methanol is hydrogenated in presence of 6.5 g of raney nickel at room temperature. After removing the catalyst the solution is concentrated and the solid filtered to give 6-amino-2-tert-butyl-5-[4-methylpiperidin-1-yl]benzothiazole melting at 146°-148°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680301
Source datasetuspto-grants-1987_07
ORD IDord-0c52bcae42524bf7a8e399ce69974129
Source noteuspto-grants-1987_07