Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635600Generated: October 27, 2026

1-Hydroxybenzotriazole → (E)-3-(6-acetamidopyridin-3-yl)-N-[2-[2,4-dichloro-N-methyl-3-[(2-methylquinolin-8-yl)oxymethyl]anilino]-2-oxoethyl]prop-2-enamide

https://huagongshe.com/reaction/1635600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(E)-3-(6-Acetamidopyridin-3-YL)acrylic acidHCID 10703461—
Reactant8-[3-(N-glycyl-N-methylamino)2,6-dichlorobenzyloxy]-2-methylquinolineHCID 11795484—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(E)-3-(6-acetamidopyridin-3-yl)-N-[2-[2,4-dichloro-N-methyl-3-[(2-methylquinolin-8-yl)oxymethyl]anilino]-2-oxoethyl]prop-2-enamideHCID 531110853.8%

Reaction Steps

To a mixture of 8-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-2-methylquinoline (100 mg), (E)-3-(6-acetamidopyridin-3-yl)acrylic acid (56.1 mg) and N,N-dimethylformamide (2 ml) were added 1-hydroxy-benzotriazole (43.4 mg) and 1-ethyl-3-(3-dimethylamino-propyl)carbodiimide hydrochloride (56.9 mg) in a nitrogen stream at 0° C., and the resulting mixture was stirred at ambient temperature for 2 hours. The reaction mixture was poured into water, and extracted with chloroform. The organic layer was washed with an aqueous solution of saturated sodium hydrogencarbonate, water and brine successively, and dried over magnesium sulfate, and thereafter the solvent was removed under reduced pressure. The residue was purified by preparative thin-layer chromatography (methanol:dichloromethane=1:10, v/v), and solidified with diethyl ether and ethyl acetate to give 8-[3-[N-[(E)-3-(6-acetamidopyridin-3-yl)acryloyl-glycyl]-N-methylamino]-2,6-dichlorobenzyloxy]-2-methyl-quinoline (FR173657) (78.8 mg) as a grayish white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509468B1
Source datasetuspto-grants-2003_01
ORD IDord-246468920e4a40358f9080d502dabd02
Source noteuspto-grants-2003_01