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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037851Generated: October 27, 2026

2,1,3-Benzoxadiazol-4(5H)-one, 5-bromo-6,7-dihydro- → 4,5-Dihydro[1,3]thiazolo[4,5-e][2,1,3]benzoxadiazol-7-amine hydrobromide

https://huagongshe.com/reaction/1037851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,1,3-Benzoxadiazol-4(5H)-one, 5-bromo-6,7-dihydro-HCID 572916—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
Product4,5-Dihydro[1,3]thiazolo[4,5-e][2,1,3]benzoxadiazol-7-amine hydrobromideHCID 8661890890%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of commercially available 5-bromo-6,7-dihydro-5H-benzo[1,2,5]oxadiazol-4-one (1.1 g, 5.1 mmol) in absolute ethanol (60 mL) was added thiourea. The reaction mixture was stirred at 60° C. for overnight and then concentrated. The residue was triturated in hexanes to afford 1.3 g (90%) of the title compound MS (ESI+) m/z 195 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546583B2
Source datasetuspto-grants-2013_10
ORD IDord-c95b0ed29fda43e196dcc79686db63e6
Source noteuspto-grants-2013_10