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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881236Generated: November 1, 2026

Chlorosulfonyl isocyanate → Ethyl 3-ureidofuran-2-carboxylate

https://huagongshe.com/reaction/881236

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 numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-bd3fa9a4b5834e1d860bd89230228872
Source noteuspto-grants-2015_03