HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168374Generated: October 30, 2026
4-Chloro-3-nitrobenzenesulfonamide → 3-Nitro-4-[2-(3-oxo-piperazin-1-yl)-ethylamino]-benzenesulfonamide
https://huagongshe.com/reaction/2168374
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-3-nitrobenzenesulfonamide | HCID 7324 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(2-Aminoethyl)piperazin-2-one | HCID 7175991 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-Nitro-4-[2-(3-oxo-piperazin-1-yl)-ethylamino]-benzenesulfonamide | HCID 67226962 | — |
Reaction Steps
4-(2-Amino-ethyl)-piperazin-2-one (5.51 g) and triethylamine (9.07 mL, 6.59 g) were added to 1,4-dioxane (100 mL), N,N-dimethylacetamide (20 mL), and water (10 mL) and mixed until dissolved. 4-Chloro-3-nitrobenzenesulfonamide (7.00 g) was added, and the mixture was heated to 90° C. for 16 hours. The mixture was cooled and the solvent was removed under vacuum. The crude material was purified by recrystallization from 20% methanol in dichloromethane with subsequent washing of the recrystallized solid with 10% methanol in dichloromethane followed by washing with 100% dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045420B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-5f6bc73856954c02ad33f149806fc434 |
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| Source note | uspto-grants-2015_06 |
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