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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696105Generated: October 27, 2026

Hydrochloric Acid → 4-(2-Oxopiperazin-1-yl)-n-(thiazol-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/1696105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-Oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)-n-(thiazol-2-yl)benzenesulfonamideHCID 59466502—
SolventWaterHCID 962—
Product4-(2-Oxopiperazin-1-yl)-n-(thiazol-2-yl)benzenesulfonamideHCID 5946563164.3%

Reaction Steps

To a stirring solution of sodium hydroxide (1.38 g, 34.5 mmol), and H2O (5.0 mL), at 0° C., was added 4-(2-oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)-N-(thiazol-2-yl)benzenesulfonamide (5.0 g, 11.5 mmol) portionwise over 10 minutes. The mixture was stirred at ambient temperature for 30 minutes. The solution was cooled to 0° C. followed by the addition of 1.0 N HCl aqueous solution (34.5 mL, 34.5 mmol). The light yellow solution was azeotroped with MeOH (4×100 mL) at <30° C. The obtained solid was suspended in 50% MeOH in CH2Cl2 (200 mL) and stirred for 5 minutes. The mixture was filtered and the filtrate was evaporated to give the desired amine as light yellow solid (2.5 g, 7.4 mmol, 64% yield). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=339.3; tR=0.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163720B2
Source datasetuspto-grants-2012_04
ORD IDord-b416ffa1790b4a0d8e6412822ec040dc
Source noteuspto-grants-2012_04