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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421883Generated: October 30, 2026

HCID 18707107, compound → HCID 54390265, compound

https://huagongshe.com/reaction/1421883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18707107HCID 18707107—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant4-(3,4-Difluorophenyl)-3-(4-nitrophenyloxy-carbonyl)-2-oxo-oxazolidineHCID 22049087—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54390265HCID 54390265—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-(3,4-difluoro-phenyl)-2-oxo-oxazolidine-3-carboxylic acid 4-nitrophenyl ester (80 mg, 0.21 mmol) in 5 ml of THF was added (4-cyano-4-phenyl-cyclohexyl)-piperidin-4-yl-carbamic acid tert-butyl ester (150 mg, 0.40 mmol) in a portion and the resulting solution was stirred for 12 h at 25° C. Reaction mixture was concentrated in vacuo, yielding a yellow oil, which was subjected to column chromatography (50% Hexane/EtOAc) to provide the tert-butyl ester of the desired product as a colorless oil. The product obtained was dissolved in 5 ml of EtOAc and 1 ml of 1N HCl-Et2O to afford a white solid of the product as the HCl salt: mp 181-192 C; Anal. Calc. For C27H28F2N4O3.1.0HCl requires C, 61.70; H, 5.73; N, 10.28. Found: C, 59.48; H, 5.41; N, 10.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080760
Source datasetuspto-grants-2000_06
ORD IDord-4286f470ffbb4457a17d0f47dcde7a1e
Source noteuspto-grants-2000_06