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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010675Generated: October 30, 2026

Boron tribromide → HCID 178465303, compound

https://huagongshe.com/reaction/1010675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 57813639HCID 57813639—
SolventDichloromethaneHCID 6344—
ProductHCID 178465303HCID 1784653037.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-ethyl-3-[7-(2-methoxy-thiazol-4-yl)-5-pyridin-3-yl-benzothiazol-2-yl]-urea (0.05 g, 0.12 mmol) in dry DCM (5 mL) was added BBr3 (0.20 mL) under nitrogen atmosphere at 0° C. The reaction mixture was then heated at 50° C. for 24 h under nitrogen atmosphere. After the completion of the reaction (TLC monitoring), the reaction mixture was cooled to 0° C. and then quenched with ice-cold water followed by extraction 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 (230-400 M) using DCM-MeOH (96:4) to provide the title compound as light greenish solid (3.5 mg, 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977340B2
Source datasetuspto-grants-2011_07
ORD IDord-e04716ffa4a848ac8d76e66e417bc523
Source noteuspto-grants-2011_07