HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12170Erstellt: 23. Oktober 2026
Toluene → 2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamide
https://huagongshe.com/de/reaction/12170
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 2-Amino-5-chloropyridine | HCID 66174 | — |
| Edukt | 5-Chloroisatoic anhydride | HCID 78480 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamide | HCID 21906418 | — |
Reaktionsschritte
To a solution of 2-amino-5-chloropyridine (787 mg, 6.1 mmol) in tetrahydrofuran (5 ml) was added 0.5M potassium bis(trimethylsilyl)amide in toluene (20 ml, 10.1 mmol) dropwise at −78° C. After stirred for additional 0.5 hr at −78° C., the mixture was added 5-chloroisatoic anhydride (1 g, 5.1 mmol) at −78° C. The mixture was warmed up to r.t gradually and stirred overnight. After concentrated, the crude was washed with saturated ammonium chloride solution and extracted by ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide as yellow solid (1.39 g. 99%). MS found for C12H9Cl2N3O M+=282, (M+2)+=284.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07727981B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-94770809738c4b598943bd373eeaa201 |
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| Quellennotiz | uspto-grants-2010_06 |
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