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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733935Generated: October 31, 2026

HCID 54177412, compound → HCID 67734520, compound

https://huagongshe.com/reaction/1733935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54177412HCID 54177412—
ReactantHCID 85722021HCID 85722021—
SolventAmmoniaHCID 222—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67734520HCID 67734520—

Reaction Steps

1 g of ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-4-methanesulfonyloxypiperidine-4-acetate (obtainable from the 4-hydroxy compound (see Example 13) with methanesulfonyl chloride/pyridine) is dissolved in a 2% NH3 solution in 10 ml of a 1:1 mixture of ethanol and THF, and the solution is left to stand at 20° for 2 hours. The solution is concentrated by evaporation and subjected to conventional work-up to give ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)-4-aminopiperidine-4-acetate, FAB 387.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532255
Source datasetuspto-grants-1996_07
ORD IDord-45358369e5474b48988130640b0eebc1
Source noteuspto-grants-1996_07