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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419236Generated: November 2, 2026

Pyridine → HCID 178511920, compound

https://huagongshe.com/reaction/1419236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Amidino-1-carbamoylmethyl-2-naphthol.hydrochlorideHCID 136454270—
ReactantHCID 178478897HCID 178478897—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventHCID 131721206HCID 131721206—
ProductHCID 178511920HCID 17851192048.8%

Reaction Steps

30 Milliliters of 20% hydrous pyridine was added to 1.71 g of 4-[(2-piperidinoethyl)aminoiminomethylamino]benzoic acid.dihydrochloride, 1.2 g of 6-amidino-1-carbamoylmethyl-2-naphthol.hydrochloride, 1.06 g of DCC and 52.4 mg of DMAP, followed by stirring for 2 hours under cooling with ice and then 4 days at room temperature. The precipitate was filtered and the filtrate was concentrated under reduced pressure. To the residue was added 15 ml of DMF, and the solution was added dropwise to a mixed liquid of 300 ml of acetone and 100 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-formic 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 2.1 ml of concentrated hydrochloric acid, and the solution was added dropwise to 450 ml of acetone, followed by stirring for 30 minutes under cooling with ice. Then, the precipitate was collected by filtration to obtain 1.08 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885990
Source datasetuspto-grants-1999_03
ORD IDord-8fb51115dbea4ecd8328abd225a85b66
Source noteuspto-grants-1999_03