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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131504Erstellt: 24. Oktober 2026

Fluoroacetyl chloride → (S)-2-Fluoro-1-[2-(2-methoxy-ethyl)-4-(2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulen-10-yl)-piperazin-1-yl]-ethanone

https://huagongshe.com/de/reaction/131504

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFluoroacetyl chlorideHCID 9663—
EduktDiisopropylethylamineHCID 81531—
EduktHCID 135457486HCID 135457486—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-2-Fluoro-1-[2-(2-methoxy-ethyl)-4-(2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulen-10-yl)-piperazin-1-yl]-ethanoneHCID 136090351—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Add a solution of fluoroacetyl chloride (0.133 g, 1.38 mmol) in anhydrous dichloromethane (1-2 mL) dropwise to a 0° C. solution of (S)-10-[3-(2-Methoxy-ethyl)-piperazin-1-yl]-2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene (0.283 g, 0.688 mmol) and diisopropylethylamine (0.240 mL, 1.38 mmol) in anhydrous dichloromethane, and stir at 0° C. for 3 hours. Concentrate the reaction under reduced pressure to afford an oil. Purify the oil by flash chromatography, eluting with a gradient of a solution of 2% 2M ammonia in methanol, in dichloromethane (0-100% in dichloromethane over 30 minutes, then 100% for 28 minutes) to give the title compound: 0.18 g (56%). Mass spectrum (APCI+, m/e): 472 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384934B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-64d0f8c8fd9541be8b805a31be9a2ed6
Quellennotizuspto-grants-2008_06