HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 987896Erstellt: 26. Oktober 2026
2,6-Diaminopyridine → N-(6-Aminopyridin-2-yl)-2,2-dimethylpropanamide
https://huagongshe.com/reaction/987896
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,6-Diaminopyridine | HCID 8861 | — |
| Edukt | Pivaloyl chloride | HCID 62493 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-(6-Aminopyridin-2-yl)-2,2-dimethylpropanamide | HCID 15050440 | 74% |
Reaktionsschritte
To a solution of 2,6-diaminopyridine (50.0 g, 0.46 mol) in dioxane (250 mL) was added slowly (1 h) pivaloylchloride (27.9 g, 0.23 mol), dissolved in dioxane (50 mL). The resulting mixture was stirred for 2 h and the white precipitate (2,6-diaminopyridine hydrochloride) filtered off. The organic phase was evaporated to dryness in vacuo, and the crude product recrystalized from n-hexane/ethyl acetate to give the desired product (32.83 g, 74%) as colorless crystals (mp 140-141° C.). 1H NMR (DMSO-d6): δ 8.93 (s, 1H), 7.34 (t, 7.9 Hz, 1H), 7.19 (d, 7.6 Hz, 1H), 6.18 (d, 7.6 Hz, 1H), 5.75 (br. s, 2H), 1.19 (s, 9H). 13C NMR (DMSO-d6): δ 176.5, 158.5, 150.4, 138.4, 103.6, 101.5, 39.4, 27.1. FAB+ MS (m/z): 193.88 M+H+, calc. for C10H15N3O+H+ 194.1293.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06632919B1 |
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| Quelldatensatz | uspto-grants-2003_10 |
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| ORD ID | ord-0b15964d70ac498983b25d445c65cd57 |
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| Quellennotiz | uspto-grants-2003_10 |
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