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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977212Generated: October 31, 2026

Ethyl Acetate → Tert-butyl 1-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonyl}piperid-4-yl-carboxylate

https://huagongshe.com/reaction/977212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTert-butyl 1-{3-[4-(5-oxo-1,2,4-oxadiazolin-3-yl)phenyl]-2-oxo-5-oxazolidinylcarbonyl}piperidine-4carboxylateHCID 136146332—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductTert-butyl 1-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonyl}piperid-4-yl-carboxylateHCID 15340942—

Reaction Steps

1.37 g of tert-butyl 1-{3-[4-(5-oxo-1,2,4-oxadiazolin-3-yl)phenyl]-2-oxo-5-oxazolidinylcarbonyl}piperidine-4-carboxylate are dissolved in 50 ml of methanol and hydrogenated over Raney nickel. The reaction mixture is, subsequently filtered and the filtrate is concentrated in vacuo. The product obtained is treated with 20 ml of ethyl acetate, with heating, and the product, after cooling, is filtered off with suction. Tert-butyl 1-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonyl}piperid-4-yl-carboxylate is obtained, m.p. 160°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614535
Source datasetuspto-grants-1997_03
ORD IDord-897d8cdcf67d4e078c37df591e1c2bb4
Source noteuspto-grants-1997_03