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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428749Generated: October 29, 2026

Pyridine → HCID 70243369, compound

https://huagongshe.com/reaction/428749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54424107HCID 54424107—
SolventDichloromethaneHCID 6344—
ProductHCID 70243369HCID 70243369—

Reaction Steps

A solution of (S)4-)-4-[4-[5-(aminomethyl)-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester (EXAMPLE 20, Step 8, 9.45 g) in dry methylene chloride (96 mL) under N2 is treated with pyridine (5.82 mL) and acetic anhydride (3.40 mL), and the resulting mixture is stirred at ambient temperature for four hours, diluted with methylene chloride (25 mL), washed with water (25 mL), saturated aqueous sodium bicarbonate (25 mL) and saline (25 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product which is then chromatographed on silica gel (230-400 mesh, 350 g), eluting with a gradient of methanol/chloroform (2.5/97.5-7.5/92.5). Pooling and concentration of those fractions with an Rf=0.51 by TLC (methanol/chloroform, 10/90) gives the title compound, mp 144-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313307B1
Source datasetuspto-grants-2001_11
ORD IDord-d3cf72aafc6643e0b77dfb42a1beb913
Source noteuspto-grants-2001_11