Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809178Generated: October 29, 2026

Boron tribromide → 3-{[3-(4-Hydroxy-phenyl)-imidazo[1,2-a]pyrazin-8-ylamino]-methyl}-benzenesulfonamide

https://huagongshe.com/reaction/1809178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3-{[3-(4-Methoxy-phenyl)-imidazo[1,2-a]pyrazin-8-ylamino]-methyl}-benzenesulfonamideHCID 58337085—
SolventDichloromethaneHCID 6344—
Product3-{[3-(4-Hydroxy-phenyl)-imidazo[1,2-a]pyrazin-8-ylamino]-methyl}-benzenesulfonamideHCID 13599825452.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

BBr3 (2.81 mL, 1.0M in DCM, 2.81 mmol) is added to a suspension of 3-{[3-(4-Methoxy-phenyl)-imidazo[1,2-a]pyrazin-8-ylamino]-methyl}-benzenesulfonamide (0.115 g, 0.281 mmol) in DCM (3 mL) at −78° C. under nitrogen atmosphere. The reaction is allowed to warm to r.t and monitored by analytical HPLC. After 2 h the reaction is complete and is cooled to −78° C., quenched with a solution of saturated aqueous K2CO3. The reaction is diluted with AcOEt, washed with water, dried with MgSO4 anh., filtered and evaporated to give 0.058 g of 3-{[3-(4-Hydroxy-phenyl)-imidazo[1,2-a]pyrazin-8-ylamino]-methyl}-benzenesulfonamide as a brown oil (52%). No further purification was required. LC-MS m/z 396 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362018B2
Source datasetuspto-grants-2013_01
ORD IDord-d3c09daa8f024e968ab90eae0bad94b2
Source noteuspto-grants-2013_01