HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401746Erstellt: 25. Oktober 2026
Water → 4-[(1,3-Thiazol-2-ylamino)sulfonyl]-N-(2-thienylmethyl)benzamide
https://huagongshe.com/reaction/401746
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Carbonate Ion | HCID 19660 | — |
| Edukt | (2-Thienylmethyl)amine | HCID 34005 | — |
| Edukt | 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide | HCID 1019318 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Katalysator | HCID 178521658 | HCID 178521658 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Produkt | 4-[(1,3-Thiazol-2-ylamino)sulfonyl]-N-(2-thienylmethyl)benzamide | HCID 57732211 | — |
Reaktionsschritte
4-Iodo-N-1,3-thiazol-2-ylbenzenesulfonamide (Preparation 98, 200 mg, 0.5 mmol), thiophene-2-methanamine (280 uL, 2.7 mmol), hexacarbonylmolybdenum (70 mg, 0.3 mmol), palladium(II) acetate (6 mg, 0.03 mmol), and sodium carbonate (170 mg, 1.6 mmol) in water (1.1 mL, 61 mmol) was heated 30 min at 110° C. in the microwave. The reaction mixture was diluted with 1 N HCl and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was dissolved in methylene chloride/MeOH and MP-Carbonate (2.73 mmol/g loading; 1.0 g, 2.73 mmol) was added. After stirring 1 h, LC/MS analysis indicated complete capture of the target compound. The resin was washed with methylene chloride then stirred in 8:1 methylene chloride/AcOH. LC/MS analysis indicated the target compound was released from the resin (not quantified). The material was further purified on the Isco (12 g SiO2, ethyl acetate to 4:1 ethyl acetate-MeOH).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08741934B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-3bbfcf8b344b4897a6009febe1fcff52 |
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| Quellennotiz | uspto-grants-2014_06 |
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