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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470623Generated: October 29, 2026

Boron tribromide → HCID 136413216, compound

https://huagongshe.com/reaction/470623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 67395701HCID 67395701—
SolventAmmoniaHCID 222—
SolventDichloromethaneHCID 6344—
ProductHCID 136413216HCID 136413216—

Reaction Steps

Boron tribromide (0.14 mL, 1.49 mmol) was added dropwise to a cooled solution of [2-(4-{5-[2-(3,4-dimethoxy-phenyl)-vinyl]-[1,2,4]oxadiazol-3-ylmethyl}-piperidin-1-yl)-ethyl]-dimethyl-amine (compound of Example 23; 0.10 g, 0.25 mmol) in dichloromethane (5 mL) at −78° C. The reaction mixture was warmed to room temperature and stirred for 6 h. The reaction mass was quenched with methanol (2 mL) and the organic solvent was evaporated. The residue obtained was dissolved in 8% methanolic ammonia (5 mL) and the inorganic solid obtained was removed by filtration. The filtrate was concentrated and purified by column chromatography (silica gel, 3% methanol in chloroform) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629277B2
Source datasetuspto-grants-2014_01
ORD IDord-ae4192ddd75f40dfbe85c5ca675cf90d
Source noteuspto-grants-2014_01