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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382198Generated: October 30, 2026

2-Biphenyl-4-yl-furan → 1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-(2-biphenyl-4-yl-furan-5-yl)ethane-1, 2-dione

https://huagongshe.com/reaction/382198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Biphenyl-4-yl-furanHCID 11042255—
Reactant1-(4(S)-benzyl-2, 2-dimethyl-oxazolidin-3-yl)-2-(biphenyl-4-yl-1H-pyrrol-3-yl)ethane-1, 2-dioneHCID 18341258—
ReactantN-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-oxamic acid ethyl esterHCID 54056950—
Product1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-(2-biphenyl-4-yl-furan-5-yl)ethane-1, 2-dioneHCID 1834126157%

Reaction Steps

According to the procedure described in Example 13 for the preparation of 1-(4(S)-benzyl-2, 2-dimethyl-oxazolidin-3-yl)-2-(biphenyl-4-yl-1H-pyrrol-3-yl)ethane-1, 2-dione, 2-biphenyl-4-yl-furan was deprotonated and alkylated with N-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-oxamic acid ethyl ester to give in 57% yield 1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-(2-biphenyl-4-yl-furan-5-yl)ethane-1, 2-dione as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306892B1
Source datasetuspto-grants-2001_10
ORD IDord-bb4995a804f3489ea59df20ad0245baf
Source noteuspto-grants-2001_10