HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Biphenyl-4-yl-furan | HCID 11042255 | — |
| Reactant | 1-(4(S)-benzyl-2, 2-dimethyl-oxazolidin-3-yl)-2-(biphenyl-4-yl-1H-pyrrol-3-yl)ethane-1, 2-dione | HCID 18341258 | — |
| Reactant | N-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-oxamic acid ethyl ester | HCID 54056950 | — |
| Product | 1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-(2-biphenyl-4-yl-furan-5-yl)ethane-1, 2-dione | HCID 18341261 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06306892B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-bb4995a804f3489ea59df20ad0245baf |
| Source note | uspto-grants-2001_10 |