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HRID 628003Erstellt: 25. Oktober 2026

Dimethylformamide → 3-Methylcarboxy-6,7-dihydropyrido[3,2-b]thieno[2,3-d]oxepine

https://huagongshe.com/reaction/628003

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
EduktTriphenylphosphineHCID 11776—
EduktMethyl 6-iodo-5-(2-(thiophen-3-yl)ethoxy)nicotinateHCID 57900415—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
Produkt3-Methylcarboxy-6,7-dihydropyrido[3,2-b]thieno[2,3-d]oxepineHCID 6686930052,8%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 6-Iodo-5-(2-thiophen-3-yl-ethoxy)-nicotinic acid methyl ester (4.40 g, 11.3 mmol) in N,N-Dimethylformamide (176 mL, 2270 mmol) was added potassium carbonate (9.37 g, 67.8 mmol), triphenylphosphine (1.19 g, 4.52 mmol) and palladium acetate (508 mg, 2.26 mmol). The reaction mixture was stirred at 90° C. 8 h. The reaction mixture was diluted with MeOH then filtered through celite. The filtrate was concentrated. The crude product was purified by flash chromatography EtOAc/Hex (0-100%) (product eluted at 30%) to give 3-methylcarboxy-6,7-dihydropyrido[3,2-b]thieno[2,3-d]oxepine (52.8%). MS: (ESI+) 262.0

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09309265B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-f67f708bc7094f0bbb33c86a7e42f08e
Quellennotizuspto-grants-2016_04