HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874530Erstellt: 24. Oktober 2026
Ethanol → N-{3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]phenyl}-3-methylpyridine-2-carboxamide
https://huagongshe.com/de/reaction/1874530
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Hydroxylamine HCl | HCID 21645 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Ethyl{[5-(3-{[(3-methylpyridin-2-yl)carbonyl]amino}phenoxy)pyridin-2-yl]carbamothioyl}carbamate | HCID 57749212 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-{3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]phenyl}-3-methylpyridine-2-carboxamide | HCID 57749272 | 84,6% |
Reaktionsschritte
A mixture of ethyl{[5-(3-{[(3-methylpyridin-2-yl)carbonyl]amino}phenoxy)pyridin-2-yl]carbamothioyl}carbamate (2.00 g, 4.43 mmol), hydroxylammonium chloride (3.13 g, 45.0 mmol), N,N-diisopropylethylamine (4.70 mL, 26.9 mmol), ethanol (50 mL) and methanol (50 mL) was stirred at 80° C. for 5 hr. The reaction solution was concentrated under reduced pressure, and ethyl acetate was added to the residue. The mixture was washed with aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was washed with ethyl acetate to give the title compound (1.35 g, 84%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08304557B2 |
|---|
| Quelldatensatz | uspto-grants-2012_11 |
|---|
| ORD ID | ord-8e6cc0b681c94bcfb529bf2a39f59fa8 |
|---|
| Quellennotiz | uspto-grants-2012_11 |
|---|