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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419233Generated: October 31, 2026

Pyridine → HCID 178511921, compound

https://huagongshe.com/reaction/1419233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Amidino-1-carbamoylmethyl-2-naphthol.hydrochlorideHCID 136454270—
ReactantHCID 178478898HCID 178478898—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventHCID 131721206HCID 131721206—
ProductHCID 178511921HCID 17851192149.4%

Reaction Steps

30 Milliliters of 20% hydrous pyridine was added to 1.2 g of 4-[(2-morpholinoethyl)aminoiminomethylamino]benzoic acid.dihydrochloride, 1.72 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 48 hours 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 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-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 15 ml of methanol and 2.2 ml of concentrated hydrochloric acid, and the solution was added dropwise to 450 ml of acetone, followed by stirring for 15 minutes under cooling with ice. Then, the precipitate was collected by filtration to obtain 840 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885990
Source datasetuspto-grants-1999_03
ORD IDord-04bcec2832314089b9da6ef92d7f032f
Source noteuspto-grants-1999_03