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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55785Erstellt: 25. Oktober 2026

Potassium Carbonate → 3-Chloro-4-(6-methoxyquinolin-2-yl)benzoic acid

https://huagongshe.com/reaction/55785

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloro-6-methoxyquinolineHCID 83647—
EduktSimtuzumabHCID 17750227—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDegme H2OHCID 49835946—
Produkt3-Chloro-4-(6-methoxyquinolin-2-yl)benzoic acidHCID 6698006346%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 2-chloro-6-methoxyquinoline (Intermediate 1) (200 mg, 1.04 mmol), 4-carboxy-2-chlorophenylboronic acid (247 mg, 1.24 mmol) and K2CO3 (369 mg, 2.70 mmol) in DEGME/H2O (7.0 mL/2.0 mL) was degassed three times under N2 atmosphere. Then PdCl2(dppf) (75 mg, 0.104 mmol) was added and the mixture was heated to 110° C. for 3 hours under N2 atmosphere. The reaction mixture was diluted with EtOAc (100 mL) and filtered. The filtrate was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give 3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid (150 mg, yield 46%) as a yellow solid, which was used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09433618B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-3219bbed21a1411293876a5c8f2bfaf0
Quellennotizuspto-grants-2016_09