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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646553Generated: November 2, 2026

Oxalyl chloride → HCID 15010821, compound

https://huagongshe.com/reaction/1646553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantFuran-3-carboxamideHCID 17914258—
SolventDichloromethaneHCID 6344—
ProductHCID 15010821HCID 15010821—

Reaction Steps

3-Furancarboxamide (167 mg) was 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180738
Source datasetuspto-grants-1993_01
ORD IDord-e8f13d73b6764a40861103cf75b9ddc0
Source noteuspto-grants-1993_01