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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274745Generated: October 31, 2026

Hydrochloric Acid → HCID 178474857, compound

https://huagongshe.com/reaction/2274745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178474856HCID 178474856—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178474857HCID 17847485790.2%

Reaction Steps

To a stirred suspension of 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 (3.5 g, 7.75 mmol) in methanol (4 mL) and ethyl acetate (17.5 mL) was added 4.0 N hydrogen chloride in dioxane (8.0 mL). The resulting mixture was stirred for 8 h, the solvent removed under reduced pressure and the residue dried in vacuo. The residue was suspended in 10% methanol in acetonitrile (17.5 mL) and stirred at room temperature for 1 h. The solid was filtered, washed with 10% methanol in acetonitrile (17.5 mL) and dried under reduced pressure at 45° C. to afford the title compound (3.32 g, 90.2%) as a crystalline solid which was characterized by XRPD. FIG. 1 shows a characteristic X-ray powder diffraction (XRPD) pattern of 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 monohydrochloride. Characteristic peaks, expressed in degrees 2θ, are listed in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126991B2
Source datasetuspto-grants-2015_09
ORD IDord-22a5b7a16aff4dd6b1d36c3a465aeaa5
Source noteuspto-grants-2015_09