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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2-Oxo-4-(2,2,2-trifluoroacetyl)piperazin-1-yl)-n-(thiazol-2-yl)benzenesulfonamide | HCID 59466502 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Oxopiperazin-1-yl)-n-(thiazol-2-yl)benzenesulfonamide | HCID 59465631 | 64.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163720B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-b416ffa1790b4a0d8e6412822ec040dc |
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| Source note | uspto-grants-2012_04 |
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