Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759401Generated: November 2, 2026

2,3-Dihydro-6-nitroimidazo(2,1-b)benzothiazole → 2,3-Dihydroimidazo(2,1-b)benzothiazol-6-amine

https://huagongshe.com/reaction/1759401

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro-6-nitroimidazo(2,1-b)benzothiazoleHCID 12891964—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2,3-Dihydroimidazo(2,1-b)benzothiazol-6-amineHCID 658687—

Reaction Steps

A mixture of 11 parts of 2,3-dihydro-6-nitroimidazo-[2,1-b]benzothiazole and 80 parts of methanol is hydrogenated at normal pressure and at room temperature with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is crystallized from dimethylbenzene. The product is filtered off and dried, yielding 5.6 parts of 2,3-dihydroimidazo[2,1-b]benzothiazol-6-amine; mp. 204°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340738
Source datasetuspto-grants-1982_07
ORD IDord-c530975a21984dfb9fcd1b3ba3763749
Source noteuspto-grants-1982_07