Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410563Generated: October 25, 2026

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

https://huagongshe.com/reaction/1410563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-methoxyquinolineHCID 83647—
ReactantSimtuzumabHCID 17750227—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthyl AcetateHCID 8857—
SolventDegme H2OHCID 49835946—
Product3-Chloro-4-(6-methoxyquinolin-2-yl)benzoic acidHCID 6698006346%

Reaction Conditions

Temperature110 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921562B2
Source datasetuspto-grants-2014_12
ORD IDord-60b636c6ddd14bfebcda2415c1fcb0df
Source noteuspto-grants-2014_12