HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 524988Erstellt: 25. Oktober 2026
Sodium Thiosulfate → 1-Amino-N-phenyl-1H-imidazole-2-carboxamide
https://huagongshe.com/reaction/524988
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Thiosulfate | HCID 24477 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Diphenylphosphinamide | HCID 853560 | — |
| Edukt | N-phenyl-1H-imidazole-2-carboxamide | HCID 2822525 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-Amino-N-phenyl-1H-imidazole-2-carboxamide | HCID 21104352 | 76% |
Reaktionsschritte
0.430 g (10.75 mmol) of sodium hydride (60% dispersion in mineral oil) was added to a 0° C. cooled solution of N-phenyl-1H-imidazole-2-carboxamide (1.55 g, 8.27 mmol) in DMF (50 mL). The mixture was stirred at 0° C. for 30 minutes and 2.70 g (11.57 mmol) of DPPONH2 (P,P-diphenylphosphinic amide, available from Sigma Aldrich®, cat. no. 5994-87-6) were added portionwise. A thick suspension formed and additional 100 mL of DMF were added. The mixture was stirred at room temperature for 3 hours and then it was poured into 150 mL of a saturated aqueous solution of sodium thiosulphate and extracted with ethyl acetate. The combined organic layer was dried over sodium sulphate, filtered and concentrated. The crude product was purified by flash chromatography (20% to 40% AcOEt/Hexanes) to yield 1.27 g (76% yield) of the title compound as a pale yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09340547B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-d0cc1334dd974c8cafb4870783af19a5 |
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| Quellennotiz | uspto-grants-2016_05 |
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