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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778390Generated: November 3, 2026

Pyridine → HCID 66685312, compound

https://huagongshe.com/reaction/1778390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Bromo-4-fluorobenzene-1-sulfonyl chlorideHCID 2778216—
ReactantHCID 66686367HCID 66686367—
SolventDichloromethaneHCID 6344—
ProductHCID 66685312HCID 6668531280.5%

Reaction Steps

To a stirred solution of methyl 7-amino-4H-chromeno[3,4-d]isothiazole-6-carboxylate (Intermediate 74, 0.300 g) in DCM (15 mL) was added pyridine (2.5 mL), followed by 2-bromo-4-fluorobenzenesulfonyl chloride (0.468 g). The resultant mixture was stirred at room temperature overnight. A further amount of 2-bromo-4-fluorobenzenesulfonyl chloride (0.300 g) was added and stirring was continued overnight. The mixture was diluted with DCM and washed with 0.5M hydrochloric acid and aqueous sodium bicarbonate. The organic layer was dried (Na2SO4), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 15-45% to give methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4H-chromeno[3,4-d]isothiazole-6-carboxylate (0.460 g) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-ac28aee2c0104a1c9ed4062eb989f762
Source noteuspto-grants-2016_02