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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1526746Erstellt: 26. Oktober 2026

Sodium Carbonate → 4-(7-chloro-1H-indazol-5-yl)-isoquinoline

https://huagongshe.com/reaction/1526746

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktIsoquinoline-4-boronic acidHCID 3761204—
Edukt5-Bromo-7-chloro-1H-indazoleHCID 21102194—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt4-(7-chloro-1H-indazol-5-yl)-isoquinolineHCID 6899799672,1%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of isoquinolin-4-ylboronic acid (1.00 g, 5.78 mmol), 5-bromo-7-chloro-1H-indazole (892 mg, 3.85 mmol), 2.0 M sodium carbonate (3.85 mL, 7.71 mmol) and dimethoxyethane was degassed with argon. Tetrakis(triphenylphosphine)palladium(0) (233 mg, 0.193 mmol) was added, the mixture degassed again with argon, then heated to 85° C. for 24 hours. The reaction was cooled and partitioned between ethyl acetate and water, the organic layer washed with and dried with sodium sulfate. The solvent was removed under vacuum and the residue purified by column chromatography (9/1 to 6/4 hexanes/ethyl acetate gradient) to give 4-(7-chloro-1H-indazol-5-yl)-isoquinoline (777 mg, 72%): 1H NMR (300 MHz, CDCl3) δ 10.52 (s, 1H) 9.31 (s, 1H), 8.53 (s, 1H), 8.22 (s, 1H), 8.09 (dd, J=7.4, 1.62 Hz, 1H), 7.28 (dd, J=7.4, 1.2 Hz, 1H), 7.87 (d, J=9.0 Hz, 1H), 7.81 (d, J=1.2 Hz, 1H), 7.72-7.64 (m, 2H), 7.57 (d, J=1.3 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085531B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-b233d54b371d42879c60d199f8080a30
Quellennotizuspto-grants-2015_07