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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1272928Erstellt: 26. Oktober 2026

Dichloromethane → 3-(3-Aminophenyl)-1-perhydro-2h-pyran-2-yl-1h-indazole5-carboxamide

https://huagongshe.com/reaction/1272928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt3-Aminophenylboronic acidHCID 92269—
Edukt3-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxamideHCID 22479915—
KatalysatorFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt3-(3-Aminophenyl)-1-perhydro-2h-pyran-2-yl-1h-indazole5-carboxamideHCID 2247995988%

Reaktionsschritte

To a solution of 3-bromo-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamide (0.500 g, 1.54 mmol) in 15 mL of ethylene glycol dimethyl ether, was added 3-aminophenyl boronic acid (0.358 g, 2.31 mmol), [1,1′-bis(diphenylphosphino)-ferrocene] complex with dichloromethane (1:1) (0.178 g, 0.098 mmol), and potassium phosphate (1.63 g, 7.7 mmol). The reaction mixture was heated to reflux temperature of the solvent for 18 hours. The solvent was then removed under reduced pressure and the crude was partitioned between ethyl acetate and water. The title compound was purified by column chromatography (SiO2, 6% MeOH in CH2Cl2) (0.457 g, 88% yield): ES-MS (m/z) 337 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07208513B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-be57060ec87845a58149d13412cef9f2
Quellennotizuspto-grants-2007_04