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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5787Generated: October 26, 2026

Thiophosgene → 2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole

https://huagongshe.com/reaction/5787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophosgeneHCID 10040—
ReactantPotassium BicarbonateHCID 516893—
Reactant6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 19794186—
SolventChloroformHCID 6212—
Product2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazoleHCID 15610362—

Reaction Steps

To a cooled mixture of 2.1 g of 6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole and 2.8 g of potassium bicarbonate in 20 ml of chloroform is added dropwise 1.6 g of thiophosgene in 5 ml of chloroform under stirring. The stirring is continued for 2 hours maintaining the temperature at 0°-2° . The solid is filtered and the filtrate is evaporated. The solid thus obtained is dissolved in chloroform and filtered through a silica gel column. The filtrate is evaporated to give 2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole, melting at 54°-58°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246927
Source datasetuspto-grants-1993_09
ORD IDord-6cc07c4d63d84829877b5eb5f5957d9d
Source noteuspto-grants-1993_09