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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBromineHCID 24408—
Reactant1-(6-Bromo-7-hydroxy-2-benzothiazolyl)-3-ethylureaHCID 21985595—
SolventAcetic AcidHCID 176—
Product1-(4,6-Dibromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-ureaHCID 21985651—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-2f5cc1a1e92a4c30a33e6ae5e6746e67
Source noteuspto-grants-2006_08