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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419251Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 178511909, compound

https://huagongshe.com/reaction/1419251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantMethanesulfonateHCID 85257—
Reactant6-Amidino-1-(2-carbamoylethyl)-2-naphtholHCID 136029813—
ReactantHCID 178514393HCID 178514393—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
ProductHCID 178511909HCID 17851190952.3%

Reaction Steps

100 Milliliters of 20% hydrous pyridine was added to 3.16 g of 4-aminoiminomethylaminobenzoic acid.methanesulfonate, 2.94 g of 6-amidino-1-(2-carbamoylethyl)-2-naphthol and 4.54 g of DCC, followed by stirring for 2 hours under cooling with ice and 24 hours at room temperature. The precipitate was filtered and the filtrate was concentrated under reduced pressure. To the residue was added 20 ml of DMF. The resulting solution was added dropwise to 500 ml of acetone, followed by stirring for 24 hours under cooling with ice. Then, the precipitate was collected by filtration to obtain a crude product. To the collected precipitate was added 150 ml of methanol to dissolve the precipitate. To the solution was added 3 g of active carbon, followed by stirring for 30 minutes at room temperature. Insoluble matter was filtered off and the filtrate was concentrated under reduced pressure. To the residue was added 30 ml of methanol to dissolve the residue with heating. The resulting solution was added dropwise to 400 ml of acetone, followed by stirring for 24 hours under cooling with ice. Then, the precipitate was collected by filtration to obtain 2.5 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885990
Source datasetuspto-grants-1999_03
ORD IDord-011d02fc700a4f16a5492395c94c3c92
Source noteuspto-grants-1999_03