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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884948Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86651053, compound

https://huagongshe.com/reaction/884948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-Chloropyridine-4-carboxylic acidHCID 2735816—
Reactant2-Amino-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenolHCID 86651065—
SolventPyridineHCID 1049—
ProductHCID 86651053HCID 8665105379.8%

Reaction Steps

To a mixture of 0.58 g of WSC and 5 ml of pyridine 5m1, 0.48 g of 3-chloroisonicotinic acid was added. The reaction mixture was stirred at room temperature for 25 minutes. To the reaction mixture, 0.75 g of 2-amino-4-(heptafluoroisopropyl)phenol was added and was stirred while heating at 60° C. for three hours. The reaction mixture was cooled to room temperature, the 0.24 g of 3-chloroisonicotinic acid and 0.29 g of WSC was added and stirred while heating at 60° C. for 1.5 hours and then at 80° C. for 1.3 hours. The mixture reaction was cooled to room temperature, and then concentrated under reduced pressure. Then, water was added to the residue, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.90 g of 3-chloro-N-[2-hydroxy-5-(heptafluoroisopropyl)phenyl]isonicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242133B2
Source datasetuspto-grants-2012_08
ORD IDord-4f7a405f31904e39a475adea5459ba2d
Source noteuspto-grants-2012_08