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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262999Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 178512531, compound

https://huagongshe.com/reaction/1262999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Carbamimidoylnaphthalen-2-yl methanesulfonateHCID 13050560—
ReactantHCID 178479383HCID 178479383—
SolventPyridineHCID 1049—
ProductHCID 178512531HCID 178512531183.7%

Reaction Steps

To 100 ml of pyridine, were added 8.6 g of 4-guanidinobenzoic acid hydrochloride and 9.0 g of DCC. The mixture was stirred for one hour under cooling in ice (reaction mixture A). To 100 ml of pyridine, was added 113 g of 6amidino-2-naphthol methanesulfonate. To the mixture, while being cooled in ice and stirred, was added the reaction mixture A portionwise over a period of one hour. After completion of the addition, the resulting mixture was stirred for another hour under cooling in ice, then overnight at room temperature. The precipitated crystals were collected by filtration and washed with pyridine and acetone. The crystals were then dissolved in about 200 ml of water and the insoluble DCU was removed by filtration. A saturated aqueous sodium hydrogencarbonate solution was added to the filtrate to precipitate pale yellow crystals. The crystals were washed with water and acetone to obtain 15 g (79.8% yield) of 6-amidino-2-naphthyl 4-guanidinobenzoate carbonate. From this carbonate other acid addition salts may be obtained by the procedure described in method A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04454338
Source datasetuspto-grants-1984_06
ORD IDord-094fc951af9c43f19cbaf1d5919db76b
Source noteuspto-grants-1984_06