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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419230Generated: October 31, 2026

Pyridine → 6-Amidino-1-carbamoylmethyl-2-naphthyl 4-[(2-dimethylaminoethyl)aminoiminomethylamino]benzoate

https://huagongshe.com/reaction/1419230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Amidino-1-carbamoylmethyl-2-naphthol.hydrochlorideHCID 136454270—
Reactant4-[(2-Dimethylaminoethyl)aminoiminomethylamino]benzoic acid.dihydrochlorideHCID 178483855—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethyl ethyl ketone acetic acid waterHCID 131721204—
Product6-Amidino-1-carbamoylmethyl-2-naphthyl 4-[(2-dimethylaminoethyl)aminoiminomethylamino]benzoateHCID 17848385486.8%

Reaction Steps

40 Milliliters of 20% hydrous pyridine was added to 1.5 g of 4-[(2-dimethylaminoethyl)aminoiminomethylamino]benzoic acid.dihydrochloride, 1.03 g of 6-amidino-1-carbamoylmethyl-2-naphthol.hydrochloride, 1.44 g of DCC and 56 mg of DMAP, followed by stirring for 2 hours under cooling with ice and then 24 hours at room temperature. The precipitate was filtered and the filtrate was concentrated under reduced pressure. To the residue was added 15 ml of methanol, and this 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 a crude product. Then, the product was subjected to silica gel column chromatography using methyl ethyl ketone-water-acetic acid (80:15:5) as an eluent, and the desired fractions were collected and the solvent was distilled off under reduced pressure. To the residue were added 15 ml of methanol and 1.41 ml of concentrated hydrochloric acid, and the 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 1.52 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885990
Source datasetuspto-grants-1999_03
ORD IDord-815d03e3193e49fc8c34386c7dc2c65c
Source noteuspto-grants-1999_03