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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865372Generated: November 1, 2026

Pyridine → HCID 9863078, compound

https://huagongshe.com/reaction/865372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 10040744HCID 10040744—
SolventDichloromethaneHCID 6344—
ProductHCID 9863078HCID 9863078—

Reaction Steps

(±)-5-(Aminomethyl)-3-[4-(3-pyridyl)-3,5-difluorophenyl]-2-oxazolidinone (PREPARATION 7, 135 mg, 0.433 mmol) in anhydrous methylene chloride (10 ml), pyridine (143 μl, 1.77 mmol, 4 eq) and acetic anhydride (167 μl, 1.77 mmol, 4 eq) are combined. The reaction is allowed to stir at 20°-25° under nitrogen. After 2.5 hr the reaction is added to methylene chloride (30 ml) and washed with saturated sodium bicarbonate then brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to a solid. This material is purified by silica gel (70 g) chromatography eluted with methanol/chloroform (1/99-4/96 gradient). The appropriate fractions are pooled and concentrated to give the title compound, mp 218°-219°; FTIR (mull)cm-1 3347, 1742, 1679, 1648, 1563, 1409, 1247, 1022, 755; MS (EI, m/z) 347 [M+ ], 303, 275, 244, 219, 73, 56; NMR (CDCl3) 8.68, 8.59, 7.85, 7.48-7.41, 7.31, 4.87-4.79, 4.10, 3.82, 3.72-3.57, 2.03 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565571
Source datasetuspto-grants-1996_10
ORD IDord-4e39bfd5764c49d9b8436d978d9939ef
Source noteuspto-grants-1996_10