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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 519399Erstellt: 25. Oktober 2026

Sarcosine → 2-Bromo-6-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-5-yl}benzaldehyde

https://huagongshe.com/reaction/519399

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSarcosineHCID 1088—
EduktPotassium CarbonateHCID 11430—
Edukt2,6-DibromobenzaldehydeHCID 12648641—
Edukt6,7,8,9-Tetrahydrobenzo[4,5]thieno[2,3-d]pyridazin-4(3H)-oneHCID 67016553—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-Bromo-6-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-5-yl}benzaldehydeHCID 8668377760,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A 25-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 1,4-dioxane (20 mL), 8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-6-one 117c (618 mg, 3.0 mmol), 2,6-dibromobenzaldehyde (1980 mg, 7.5 mmol), CuBr (215 mg, 1.5 mmol), sarcosine (267 mg, 3.0 mmol), and K2CO3 (828 mg, 6.0 mmol). After three cycles of vacuum/argon flush, the mixture was heated at 100° C. for 16 h. After this time the reaction was cooled to room temperature. It was then filtered and the filtrate was evaporated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with 30:1 dichloromethane/methanol to afford 130a (702 mg, 60%) as a yellow solid. MS: [M+H]+ 389.0

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09115152B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-d6c6500de8a541c6a23147b9011ad863
Quellennotizuspto-grants-2015_08