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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604601Generated: October 26, 2026

1-Hydroxybenzotriazole → 8-[2,6-dichloro-3-[N-[3-[N-(3-methylcarbamoylphenyl)carbamoyl]propionyl]-N-methylamino]benzyloxy]-2-methylquinoline

https://huagongshe.com/reaction/1604601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Amino-N-methylbenzamideHCID 676526—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant8-[3-[N-(3-carboxypropionyl)-N-methylamino]-2,6-dichlorobenzyloxy]-2-methylquinolineHCID 19603338—
SolventDichloromethaneHCID 6344—
Product8-[2,6-dichloro-3-[N-[3-[N-(3-methylcarbamoylphenyl)carbamoyl]propionyl]-N-methylamino]benzyloxy]-2-methylquinolineHCID 1960339357.2%

Reaction Steps

to amixture of 8-[3-[N-(3-carboxypropionyl)-N-methylamino]-2,6-dichlorobenzyloxy]-2-methylquinoline (139 mg), 3-amino-N-methylbenzamide (51.3 mg) and anhydrous dichloromethane (4 ml) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (71.5 mg) and 1-hydroxybenzotriazole (54.6 mg). The mixture was stirred for 12 hours at ambient temperature ans washed with water. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residue was purifed by preparative thin-layer chromatography (chloroform-methanol) followed by pulverization with diethyl ether to give 8-[2,6-dichloro-3-[N-[3-[N-(3-methylcarbamoylphenyl)carbamoyl]propionyl]-N-methylamino]benzyloxy]-2-methylquinoline (103 mg) as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994368
Source datasetuspto-grants-1999_11
ORD IDord-7c427f62e5f242f7b3fd6a92bfe762b8
Source noteuspto-grants-1999_11