Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802274Generated: October 31, 2026

Boron tribromide → 2-(7-Amino-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-phenol

https://huagongshe.com/reaction/1802274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant2-(2-Methoxyphenyl)-[1,2,4]triazolo[1,5-a]pyridin-7-amineHCID 67774260—
SolventDichloromethaneHCID 6344—
Product2-(7-Amino-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-phenolHCID 13637235860%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 2-(2-methoxy-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-7-ylamine (2.3 g, 9.6 mmol) (Example 102, step c) in DCM (60 ml) was added a solution of BBr3 (1 M in DCM, 28.7 ml, 28.7 mmol). The mixture was allowed to warm up to 25° C. and stirring was continued for 2 h. Volatiles were removed under reduced pressure and the crude residue was extracted with DCM and washed with aq. NaHCO3 solution. The organic layer was washed with brine, dried over Na2SO4 and concentrated to get the crude product which was washed with 10% DCM in hexane to afford the title compound as off-white solid (1.3 g, 60%). LC-MS: m/z=227.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-89327fe6c6de412b9fb37259b93d66bf
Source noteuspto-grants-2013_01