HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 15010821, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Furan-3-carboxamide | HCID 17914258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15010821 | HCID 15010821 | — |
Reaction Steps
3-Furancarboxamide (167 mg) was suspended in dichloromethane (10 ml), followed by addition of oxalyl chloride (0.20 ml) under ice-cooling, and the temperature of the reaction mixture was raised to room temperature. The reaction mixture was refluxed for 10 hours and the solvent was distilled off to give crude 3-furoyl isocyanate. In the same manner as in Example 8, the above product was reacted with fumagillol (213 mg) with stirring at room temperature for 30 minutes. Purification by silica gel column chromatography (eluent: n-hexane-ethyl acetate=2:1) gave colorless, powdery O-[N-(3-furoyl) carbamoyl]fumagillol (120 mg) (38% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166172 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-8746a5bc77ae46b0b888571468b2da66 |
| Source note | uspto-grants-1992_11 |