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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401746Generated: October 27, 2026

Water → 4-[(1,3-Thiazol-2-ylamino)sulfonyl]-N-(2-thienylmethyl)benzamide

https://huagongshe.com/reaction/401746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantCarbonate IonHCID 19660—
Reactant(2-Thienylmethyl)amineHCID 34005—
Reactant4-Iodo-N-(thiazol-2-yl)benzenesulfonamideHCID 1019318—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 178521658HCID 178521658—
SolventHydrochloric AcidHCID 313—
Product4-[(1,3-Thiazol-2-ylamino)sulfonyl]-N-(2-thienylmethyl)benzamideHCID 57732211—

Reaction Steps

4-Iodo-N-1,3-thiazol-2-ylbenzenesulfonamide (Preparation 98, 200 mg, 0.5 mmol), thiophene-2-methanamine (280 uL, 2.7 mmol), hexacarbonylmolybdenum (70 mg, 0.3 mmol), palladium(II) acetate (6 mg, 0.03 mmol), and sodium carbonate (170 mg, 1.6 mmol) in water (1.1 mL, 61 mmol) was heated 30 min at 110° C. in the microwave. The reaction mixture was diluted with 1 N HCl and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was dissolved in methylene chloride/MeOH and MP-Carbonate (2.73 mmol/g loading; 1.0 g, 2.73 mmol) was added. After stirring 1 h, LC/MS analysis indicated complete capture of the target compound. The resin was washed with methylene chloride then stirred in 8:1 methylene chloride/AcOH. LC/MS analysis indicated the target compound was released from the resin (not quantified). The material was further purified on the Isco (12 g SiO2, ethyl acetate to 4:1 ethyl acetate-MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-3bbfcf8b344b4897a6009febe1fcff52
Source noteuspto-grants-2014_06