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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44822Erstellt: 23. Oktober 2026

Acetic Acid → 2-(1H-pyrazol-3-yl)-1,3-thiazole

https://huagongshe.com/de/reaction/44822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrazineHCID 9321—
Edukt2-AcetylthiazoleHCID 520108—
EduktN,N-dimethylformamide N,N-dimethylacetamideHCID 22628260—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(1H-pyrazol-3-yl)-1,3-thiazoleHCID 3363559100%

Reaktionsschritte

Dissolved 1-(thiazol-2-yl)ethanone (1-BA-1, 5 g, 39.7 mmole) in DMF DMA (9.5 g, 2 eq). The resulting mixture was warmed to 100° C. until all the ketone starting material was consumed. This material was concentrated under reduced pressure to give 6.5 g of crude intermediate. This material was dissolved in 25 mL of DCM and 5 mL of HOAc was added, followed by hydrazine (5 g, 4 eq) at 0° C. The resulting mixture was heated at reflux until all the starting material was consumed. The reaction mixture was cooled to rt and neutralized with 30 mL of a saturated NaHCO3 solution. The layers were separated and the aqueous layer was extracted with DCM (2×50 mL). The organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The crude material was purified by MPLC (eluted with 0-20% MeOH/DCM) to give 2-(1H-pyrazol-5-yl)thiazole (Compound 2-BA-1, ˜6 g). LC/MS: 152.0 m/z (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541418B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-33c7b881441d4f7ba523444091fcca09
Quellennotizuspto-grants-2013_09