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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447046Generated: October 30, 2026

Boron tribromide → HCID 178465302, compound

https://huagongshe.com/reaction/447046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant1-Ethyl-3-[7-(6-methoxy-pyridin-2-yl)-5-pyridin-3-yl-benzothiazol-2-yl]-ureaHCID 57813590—
SolventDichloromethaneHCID 6344—
ProductHCID 178465302HCID 178465302—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-ethyl-3-[7-(6-methoxy-pyridin-2-yl)-5-pyridin-3-yl-benzothiazol-2-yl]-urea (0.04 g, 0.098 mmol) in dry DCM was added BBr3 (0.50 ml) under nitrogen atmosphere at 0° C. The reaction mixture was then heated at 50° C. for 6 h under nitrogen atmosphere. Since the starting material was not consumed (TLC monitoring), toluene (5 mL) was added into the reaction mixture and heated at 120° C. for 16 h. After the completion of the reaction (TLC monitoring), the reaction mixture was cooled to 0° C. and quenched with ice-cold water. Toluene was distilled off, added water and extracted with DCM. The combined organic layers were dried over anhydrous Na2SO4, and evaporated to dryness under reduced pressure. The crude residue was purified over silica gel (100-200 M) using DCM-MeOH (96:4) to provide the title compound as off white solid (2.5 mg, 6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481544B2
Source datasetuspto-grants-2013_07
ORD IDord-9bf4b6afd1d645e7a878965b48fcd972
Source noteuspto-grants-2013_07