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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359924Generated: November 1, 2026

Methanesulfonamide → HCID 66634153, compound

https://huagongshe.com/reaction/2359924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-Bromo-1,3-thiazole-2-carboxylic acidHCID 15122065—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66634153HCID 66634153—

Reaction Steps

4-Bromo-1,3-thiazole-2-carboxylic acid (1.0 g, 4.8 mmol) were initially charged in tetrahydrofuran (10 ml). N,N′-Carbonyldiimidazole (1.17 g, 7.2 mmol) was added and the reaction mixture was heated under reflux for 1 h. Methanesulphonamide (0.69 g, 7.2 mmol) was added and, after 10 min, 1,8-diazabicyclo[5.4.0]undec-7-ene (1.10 g, 7.2 mmol). The reaction mixture was stirred at room temperature for 16 h and then the solvent was removed under reduced pressure. The residue was taken up in water and acidified with hydrochloric acid. The precipitated product was filtered off with suction. This gave 1.18 g (84% of theory) of 4-bromo-N-(methylsulphonyl)-1,3-thiazole-2-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686004B2
Source datasetuspto-grants-2014_04
ORD IDord-0f645b2fd7de41bb8fcdc72664d68022
Source noteuspto-grants-2014_04