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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065674Generated: October 26, 2026

Hydrochloric Acid → 2-{1-Carboxy-2-[4-(quinolin-4-ylamino)-phenyl]-ethylamino}-6-chloro-quinoline-3-carboxylic acid

https://huagongshe.com/reaction/2065674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dichloroquinoline-3-carboxylic acidHCID 24266068—
Reactant2-Amino-3-[4-(quinolin-4-ylamino)-phenyl]propionic acid dihydrochloride dihydrateHCID 67360265—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-{1-Carboxy-2-[4-(quinolin-4-ylamino)-phenyl]-ethylamino}-6-chloro-quinoline-3-carboxylic acidHCID 4525653184%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2,6-dichloro-quinoline-3-carboxylic acid (0.17 g, 0.7 mmol), 2-amino-3-[4-(quinolin-4-ylamino)-phenyl]propionic acid dihydrochloride dihydrate (0.291 g, 0.7 mmol) and K2CO3 (0.507 g, 3.7 mmol) in DMSO (1.5 mL) is stirred at 110° C. temperature for 24 h in a Pierce reaction vial. After cooling the reaction mixture is diluted with water (10 mL) and acidified with 2N aqueous HCl till pH ˜3. The precipitated solid is collected on filter and washed with water to give the title compound (0.3 g, 84%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288549B2
Source datasetuspto-grants-2012_10
ORD IDord-f60ae66e9e87407994d73fdf8680c38e
Source noteuspto-grants-2012_10