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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274747Generated: November 1, 2026

Hydrogen Bromide → HCID 178419571, compound

https://huagongshe.com/reaction/2274747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantIsopropanolHCID 3776—
ReactantHCID 178474584HCID 178474584—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 178419571HCID 17841957198%

Reaction Steps

To a suspension of N-[3-(2-Fluoro-4′-{[(1H-[1,2,3]triazol-4-ylmethyl)-amino]-methyl}-biphenyl-4-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide (20 mg, 0.046 mmol) in 1:1 methanol/dichloromethane (0.6 mL) was added dropwise 0.5 M hydrobromic acid in isopropanol (0.28 mL, 0.14 mmol). The reaction mixture was stirred overnight at room temperature. The solvent was removed under reduced pressure, acetonitrile (0.6 mL) was added and the resulting slurry stirred at room temperature overnight. The solid was filtered and dried to give the title compound (0.6 g, 98%) as a solid which was characterized by XRPD. FIG. 3 shows a characteristic X-ray powder diffraction (XRPD) pattern of amorphous N-{[(5S)-3-(2-fluoro-4′-{[(1H-1,2,3-triazol-5-ylmethyl)amino]methyl}biphenyl-4-yl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide monohydrobromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126991B2
Source datasetuspto-grants-2015_09
ORD IDord-345f616110c849d8b325347653380bf2
Source noteuspto-grants-2015_09