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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368921Generated: October 30, 2026

Dicyclohexylcarbodiimide → 4-[[(3-Chloro-4-methoxyphenyl)methyl]amino]-6-cyano-3-quinolinecarboxylic acid pentafluorophenyl ester

https://huagongshe.com/reaction/1368921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPentafluorophenolHCID 13041—
ReactantHCID 12069380HCID 12069380—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[[(3-Chloro-4-methoxyphenyl)methyl]amino]-6-cyano-3-quinolinecarboxylic acid pentafluorophenyl esterHCID 1206938341%

Reaction Steps

To 275 mg (0.748 mmol) of 4-[[(3-chloro-4-methoxyphenyl)-methyl]amino]-6-cyano-3-quinolinecarboxylic acid was added 276 mg (1.50 mmol, 2.0 eq) pentafluorophenol, and the mixture was dispersed in 5 mL anhydrous DMF under nitrogen. To this dispersion was added a solution of 231 mg (1.12 mmol, 1.5 eq) of dicyclohexylcarbodiimide (Aldrich) in 2 mL anhydrous ethyl acetate at RT. The resulting mixture was stirred for 18 hours. The reaction was then diluted with 10 mL EtAc, and the white precipitate was filtered and discarded. The filtrate was concentrated in vacuo, and the residue was triturated with 5% MeOH/95% CH 2Cl2 to give 164 mg (0.307 mmol, 41% yield) of the title compound as a white solid: LC/MS: M/Z 534 (M+H) observed, 100% purity; mp: decomposed 215-217° C. LC: 4.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576644B2
Source datasetuspto-grants-2003_06
ORD IDord-3a6de525bfaa475ab0703b4d006c8412
Source noteuspto-grants-2003_06