HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9119Generated: October 29, 2026
Toluene → 1-(4,6-Dibromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-urea
https://huagongshe.com/reaction/9119
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(6-Bromo-7-hydroxy-2-benzothiazolyl)-3-ethylurea | HCID 21985595 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(4,6-Dibromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-urea | HCID 21985651 | — |
Reaction Steps
To a suspension of 1-(6-bromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-urea (50 mg, 0.158 mmol) in AcOH (2 mL) at about 20° C. was added Br2 (9 μl, 0.174 mmol). The reaction mixture was stirred at about 20° C. for about 15 minutes. Toluene (10 mL) was added and the solvents evaporated. The crude material was purified by preparative LC/MS to give 19 mg (30%) pure 18. 1H NMR (DMSO) δ 1.09 (t, 3H, J=6 Hz CH3), 3.19 (m, 2H, CH2), 6.55 (br s, 1H, NH), 7.68 (s, 1H, ArH), 10.51 (br s, 1H, NH or OH), 11.20 (br s, 1H, NH or OH). HPLC retention timer 2.90 minutes.
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-2f5cc1a1e92a4c30a33e6ae5e6746e67 |
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| Source note | uspto-grants-2006_08 |
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