HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → 4-nitrobenzyl 2-[(4S)-4-phenylacetamido-3-oxo-2-isoxazolidinyl]-3-(2acetamidoethylthio)-5-oxo-2-tetrahydrofurancarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | (4S)-4-phenylacetamido-3-isoxazolidinone | HCID 56633768 | — |
| Reactant | HCID 67901886 | HCID 67901886 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-nitrobenzyl 2-[(4S)-4-phenylacetamido-3-oxo-2-isoxazolidinyl]-3-(2acetamidoethylthio)-5-oxo-2-tetrahydrofurancarboxylate | HCID 67902275 | 57.3% |
Reaction Steps
In 5 ml of dichloromethane were suspended 48 mg of (4S)-4-phenylacetamido-3-isoxazolidinone and 95 mg of the Compound (70) obtained in Example 70. To the suspension was added 71 mg of 1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline. The mixture was stirred for 5.5 hours at room temperature. The solvent was evaporated off, and the residue was subjected to a silica gel column chromatography, followed by elution with ethyl acetate to give 75 mg of the subject Compound (71) as a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04851422 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-38b7c90d32a643a0bdcd277cb8efddfe |
| Source note | uspto-grants-1989_07 |