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HRID 245637Erstellt: 25. Oktober 2026

9-Methoxy-9-borabicyclo(3.3.1)nonane → HCID 178498804, Verbindung

https://huagongshe.com/reaction/245637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt9-Methoxy-9-borabicyclo(3.3.1)nonaneHCID 544964—
EduktHCID 178418348HCID 178418348—
EduktHCID 178498803HCID 178498803—
KatalysatorBis(triphenylphosphine)palladium chlorideHCID 84124—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178498804HCID 17849880466%

Reaktionsschritte

To a solution of 899 mg (5.91 mmol) of 9-methoxy-9-bora-bicyclo[3.3.1]nonane in 5 mL of anhydrous tetrahydrofuran is added dropwise 3.71 mL (5.91 mmol) of a solution 1N of methyl lithium in diethylether. After few minutes of stirring, a mixture of 6-amino-3-bromo-5-chloro-1H-indazole-7-carboxylic acid methyl ester, prepared as in step a in example 39, and 104 mg (0.15 mmol) of bis(triphenylphosphine) palladiumI(II) dichloride in 10 mL of anhydrous tetrahydrofuran is added. The reaction mixture is stirred in a microwave oven at 150° C. for 15 minutes. After filtration over Celite and concentration in vacuo, the residue is purified by flash chromatography (SiO2, hexanes/ethyl acetate 1:1) to afford 470 mg of product (66%) as a pale yellowish solid; LC/MS:240/242 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658801B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-08bef5de52894447a2b63c14211b6865
Quellennotizuspto-grants-2014_02