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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419232Generated: October 31, 2026

Pyridine → HCID 178478766, compound

https://huagongshe.com/reaction/1419232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Amidino-1-carbamoylmethyl-2-naphthol.hydrochlorideHCID 136454270—
ReactantHCID 178479747HCID 178479747—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethyl ethyl ketone acetic acid waterHCID 131721204—
ProductHCID 178478766HCID 178478766101.2%

Reaction Steps

55 Milliliters of 10% hydrous pyridine was added to 1.5 g of 4-morpholinoaminoiminomethylamino-benzoic acid.hydrochloride, 1.12 g of 6-amidino-1-carbamoylmethyl-2-naphthol.hydrochloride, 1.55 g of DCC and 61 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 the solution was added dropwise to 400 ml of ether, 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 20 ml of methanol and 2.07 ml of concentrated hydrochloric acid, and the solution was added dropwise to a mixed liquid of 200 ml of ether and 200 ml of acetone, followed by stirring for 24 hours under cooling with ice. Then, the precipitate was collected by filtration to obtain 1.42 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885990
Source datasetuspto-grants-1999_03
ORD IDord-3940873ec88e4187b60245e26fd2550e
Source noteuspto-grants-1999_03