HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9153Generated: October 25, 2026
N-p-Bromophenylthiourea → N-[7-(4-Bromoanilino)-4,5-dihydro[1,3]thiazolo[4',5': 3,4]benzo[d][1,3]thiazol-2-yl]-N'-ethylurea
https://huagongshe.com/reaction/9153
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-p-Bromophenylthiourea | HCID 2735620 | — |
| Reactant | 1-(6-Bromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea | HCID 21985543 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[7-(4-Bromoanilino)-4,5-dihydro[1,3]thiazolo[4',5': 3,4]benzo[d][1,3]thiazol-2-yl]-N'-ethylurea | HCID 86588976 | — |
Reaction Steps
A suspension of N-(6-bromo-7-oxo-4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)-N′-ethylurea (50 mg, 0.16 mmol) and 4-bromo-phenyl-thiourea (36 mg, 0.16 mmol) in THF (1.0 mL) was heated to about 65° C. for about 1.5 hrs. The reaction mixture was pumped down and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091227B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ea8233a5c256454ba3ea6ba2c519a36d |
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| Source note | uspto-grants-2006_08 |
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