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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1868328Erstellt: 26. Oktober 2026

Dichloromethane → 1-(4-Amino-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanone

https://huagongshe.com/reaction/1868328

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktPotassium CarbonateHCID 11430—
Edukt4-MethoxybenzylamineHCID 75452—
Edukt1-(4-Chloro-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanoneHCID 18446512—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(4-Amino-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanoneHCID 10265028—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a suspension of 1-(4-chloro-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanone 97 (61 mg, 0.21 mmol) and potassium carbonate (174 mg, 1.26 mmol) in DMF (1.8 mL) was added 4-methoxybenzylamine (85 μl, 0.64 mmol). The resultant mixture was heated at 50° C. for 6.75 h. After this time, 20 mL of a 1:1 mixture of dichloromethane and methanol was added and the resultant slurry was filtered. The filtrate was concentrated and the residue was dissolved in trifluoroacetic acid (7 mL). The resultant mixture was heated at 55° C. for 2.75 h. After this time, the reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluent: dichloromethane:MeOH:Et3N, 98.5:1.5:0.5) to give 98.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07635695B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-d145112c00254d549092af405f18581f
Quellennotizuspto-grants-2009_12