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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809339Generated: October 30, 2026

Pyridine → HCID 57542144, compound

https://huagongshe.com/reaction/1809339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-AminothiazoleHCID 2155—
ReactantHCID 59432940HCID 59432940—
ProductHCID 57542144HCID 5754214471.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-(2,2,2-Trichloro-acetyl)-2,3-dihydro-1H-isoindole-5-sulfonyl chloride (0.25 g, 0.7 mmol), was added to a stirring solution of 2-aminothiazole (0.07 g, 0.7 mmol) and pyridine (57 μl, 0.7 mmol) and heated to 60° C. for 1 h. The reaction mixture was then partitioned between CH2Cl2 and aqueous 1N HCl solution. The organic layer was concentrated in vacuo and purified via silica gel chromatography (3% MeOH in CH2Cl2) to give the sulfonamide as a tan solid (200 mg, 0.5 mmol, 67% yield). LC/MS (10-99% CH3CN), M/Z: M+1 obs=426.0; tR=2.88 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362032B2
Source datasetuspto-grants-2013_01
ORD IDord-76031d09b1364923b6e14595c335a667
Source noteuspto-grants-2013_01