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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098608Generated: October 29, 2026

Chlorosulfonyl isocyanate → Ethyl 3-ureidofuran-2-carboxylate

https://huagongshe.com/reaction/2098608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-aminofuran-2-carboxylateHCID 45790120—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-ureidofuran-2-carboxylateHCID 5959313892%

Reaction Steps

To a solution of methyl 3-aminofuran-2-carboxylate 34 (100 mg, 1.0 eq) in dichloromethane (3 ml) at −78° C. was added chlorosulfonyl isocyanate (0.09 ml, 1.4 eq) dropwise. The reaction was slowly warmed to room temperature and stirred for 40 minutes. Reaction was concentrated. To the residue was added 6N HCl (3.5 ml) and mixture was heated to 100° C. for 20 minutes. Reaction mixture was allowed to cool down to room temperature, and was neutralized with saturated aq. NaHCO3. Solid was collected by filtration to yield ethyl 3-ureidofuran-2-carboxylate 35 (120 mg, 92%) as a beige solid which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-2e7e24c32ce941fbb24aec7c5fa97181
Source noteuspto-grants-2013_05