HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559511Generated: November 1, 2026
Hydrochloric Acid → HCID 86611699, compound
https://huagongshe.com/reaction/559511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67001458 | HCID 67001458 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86611699 | HCID 86611699 | 40% |
Reaction Steps
A suspension of 4-(2,5-dioxo-imidazolidin-4-yl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide (0.1 mmol), benzyl bromide (0.2 mmol), and potassium carbonate (0.1 mmol) in DMF (5 mL) was stirred at 65° C. for 4 h. The reaction mixture was acidified with 6N HCl aqueous solution and was stirred for 30 min before neutralized with saturated NaHCO3. The mixture was extracted with ethyl acetate and organic phase was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by reverse phase HPLC to give 4-(1-benzyl-2,5-dioxo-imidazolidin-4-yl)-N-thiazol-2-yl-benzenesulfonamide (0.04 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063080B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-e9afae1c1165458e8ac0fa94de1ed655 |
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| Source note | uspto-grants-2011_11 |
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