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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075808Generated: October 31, 2026

Hydrochloric Acid → HCID 57709574, compound

https://huagongshe.com/reaction/2075808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant5,7-Dichloro-4-hydroxy-quinoline-2-carboxylic acid ethyl esterHCID 826769—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 57709574HCID 57709574100.3%

Reaction Steps

A 12-L three-neck flask equipped with a mechanical mixer, a condenser, and thermocouple was charged with Compound 4 (0.94 mole, 269.1 g) in acetonitrile (ACN; about 4 L), after which chlorosulfonyl isocyanate (0.99 mole, 86 mL) was added (dropwise) via the dropping funnel. Upon completion of the addition, the resulting reaction mixture was refluxed for about 28 minutes. The pH of the mixture was about 0 at this point. The mixture then was cooled slightly, while adding saturated HCl in methanol (MeOH; 500 mL). Subsequently, the mixture was refluxed for about 1 hour, and then allowed to cool to room temperature overnight, during which time crystals formed. The crystals were collected on a sintered glass frit and rinsed with acetonitrile (400 mL and 500 mL). The filter cake was then transferred to a 12 L reactor with a mechanical stirrer. Deionized (DI) water (900 mL) and saturated Na2CO3 (500 mL) were added to afford mixture having a pH of about 10. Next, the solids in the mixture were collected and slurry rinsed with DI water (3×500 mL). The rinsed product was dried via lyophilization to afford about 268.79 g (63.3% yield) of Compound 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923458B2
Source datasetuspto-grants-2011_04
ORD IDord-35a6c801e5a146adb62fe5c49a6815bc
Source noteuspto-grants-2011_04