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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33464Erstellt: 24. Oktober 2026

Pyridine → N-(2-(piperidin-1-yl)phenyl)isoxazole-5-carboxamide

https://huagongshe.com/de/reaction/33464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt2-(Piperidin-1-yl)anilineHCID 458795—
EduktIsoxazole-5-carbonyl chlorideHCID 2736707—
EduktHOBt resinHCID 16217185—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(2-(piperidin-1-yl)phenyl)isoxazole-5-carboxamideHCID 11277266100%

Reaktionsschritte

To PS-HOBt resin (0.1 mmol) was added anhydrous dichloromethane (“DCM”) (1 mL) followed by pyridine (0.5 mmol) and isoxazole-5-carbonyl chloride (Lancaster) (0.3 mmol). The mixture was shaken at room temperature for 3 h and was then filtered. The resin was washed successively with tetrahydrofuran (“THF”) (3×) and DCM (3×) and dried in vacuo. To this acylated resin was added a solution of 2-piperidinoaniline (Lancaster) (0.05 mmol, 0.5 eq) in anhydrous THF (1 mL) and the mixture was shaken at room temperature for 16 h. The mixtue was then filtered and the resin washed with THF and DCM as described above. The combined filtrate and washings were concentrated under reduced pressure to yield the product. Yield: 100%. MS: 272 (M+1). LC/MS purity: 100%. 1HNMR (CDCl3, 300 MHz): δ 8.2 (d, 1H), 7.85 (t, 2H), 7.55 (m, 1H), 7.4 (m, 2H), 3.8-3.2 (bm, 4H), 2.7-1.9 (bm, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429603B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-cc1fc177866d45a0b0846b9269bdeffc
Quellennotizuspto-grants-2008_09