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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1352371Erstellt: 26. Oktober 2026

Dibromodifluoromethane → 4-[5-(2,2-Difluoro-vinyl)-thiazol-2-yl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1352371

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibromodifluoromethaneHCID 6382—
EduktTriphenylphosphineHCID 11776—
EduktTert-butyl 4-(5-formyl-1,3-thiazol-2-yl)piperazine-1-carboxylateHCID 23560811—
KatalysatorZincHCID 23994—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[5-(2,2-Difluoro-vinyl)-thiazol-2-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 6754954719%

Reaktionsschritte

To a solution of 6.73 mmol triphenylphosphine in 13 ml N,N-dimethylformamide was added 6.73 mmol dibromodifluoromethane and the mixture was stirred at room temperature for 1 h. 3.36 mmol 4-(5-formyl-thiazol-2-yl)-piperazine-1-carboxylic acid tert-butyl ester was added and the mixture was then cooled to 0° C. 6.73 mmol zinc dust was added in small portions and stirring continued for 10 min at 0° C. The mixture was then allowed to warm to room temperature and stirring continued for a further 2 h. The reaction mixture was then filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography (SiO2, ethyl acetate/heptane) to afford the title compound as a white crystalline solid (yield 19%). MS (m/e): 332.3 (M+H+, 10%), 276.0 ([M+2H−tBu]+, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07220744B2
Quelldatensatzuspto-grants-2007_05
ORD IDord-893b7398074045f48b844b52356d1857
Quellennotizuspto-grants-2007_05