HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78426Generated: 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/78426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,1,3-Benzoxadiazol-4(5H)-one, 5-bromo-6,7-dihydro- | HCID 572916 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,5-Dihydro[1,3]thiazolo[4,5-e][2,1,3]benzoxadiazol-7-amine hydrobromide | HCID 86618908 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841334B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-86eb7f7bb1c945d5bb9ab8c3c13b50d9 |
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| Source note | uspto-grants-2014_09 |
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