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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1472640Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1472640

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
PatentnummerUS09012646B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-305c57c7bb87415f8f3ec0848b838a06
Quellennotizuspto-grants-2015_04