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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692755Generated: November 2, 2026

Chlorosulfonyl isocyanate → HCID 57685407, compound

https://huagongshe.com/reaction/1692755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 5-amino-2-phenyl-1,3-thiazole-4-carboxylateHCID 13514498—
SolventDichloromethaneHCID 6344—
ProductHCID 57685407HCID 57685407—

Reaction Steps

To a solution of ethyl 2-phenyl-5-aminothiazole-4-carboxylate (116 mg, 1.0 eq) in dichloromethane (3 ml) at −78° C. was added chlorosulfonyl isocyanate (0.06 ml, 1.3 eq) dropwise (Redman et al J. (2000) Org. Lett. 2:2061-2063). The reaction was slowly warmed to room temperature and stirred for 40 minutes. The reaction was concentrated. To the residue was added 6N HCl (2.5 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 2-phenyl-5-ureidothiazole-4-carboxylate 63 as a beige solid which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158626B2
Source datasetuspto-grants-2012_04
ORD IDord-f05e55d51e4d4900a22dd70008ad1de9
Source noteuspto-grants-2012_04