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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470621Generated: October 29, 2026

Boron tribromide → HCID 136413215, compound

https://huagongshe.com/reaction/470621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 67397310HCID 67397310—
SolventAmmoniaHCID 222—
SolventDichloromethaneHCID 6344—
ProductHCID 136413215HCID 136413215—

Reaction Steps

Boron tribromide (0.229 mL, 2.42 mmol) was added dropwise to a cooled solution of 4-{5-[2-(3,4-Dimethoxy-phenyl)-vinyl]-[1,2,4]oxadiazol-3-ylmethyl}-1-isopropyl-piperidine (compound of Example 21; 0.15 g, 0.4 mmol) in dichloromethane (5 mL) at −78° C. The reaction mixture was warmed to room temperature and stirred for 6 h. The reaction mixture 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-20e8ec680c2747ffa8dfd12545444f56
Source noteuspto-grants-2014_01