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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455503Generated: October 31, 2026

1,2-Dichloroethane → HCID 135525315, compound

https://huagongshe.com/reaction/1455503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAnilineHCID 6115—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 9858643HCID 9858643—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 135525315HCID 135525315—

Reaction Steps

EDC (633 mg, 3.3 mmol) was added to a solution of 2-(2-Chloro-phenylamino)-7-methoxy-quinoline-3-carboxylic acid (986 mg, 3.0 mmol), HOBt (446 mg, 3.3 mmol) and aniline (307 mg, 3.3 mmol) in DMF (5 ml) at room temperature. After stirring the mixture for 1 hr, CH2Cl2 was used to extract the reaction mixture, and washed with water, saturated brine and then dried with magnesium sulfate. The solvent was removed under reduced pressure to give yellow oil. The yellow oil was purified by chromatography on SCX column using MeOH as eluent. At last, 2-(2-Chloro-phenylamino)-7-hydroxy-quinoline-3-carboxylic acid phenylamide was obtained as yellow solid after recrystallization from CH2Cl2 and Hexane; 947 mg (78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482455B2
Source datasetuspto-grants-2009_01
ORD IDord-00b0080823d042edb078e8ad7c6199fc
Source noteuspto-grants-2009_01