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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867914Generated: October 31, 2026

Pyridine → HCID 86742467, compound

https://huagongshe.com/reaction/867914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Carbamimidoylnaphthalen-2-yl methanesulfonateHCID 13050560—
ReactantHCID 86742469HCID 86742469—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetoneHCID 180—
ProductHCID 86742467HCID 8674246741.4%

Reaction Steps

To 1.03 g of 4-(2-imidazolinyl)amino-benzoic acid methanesulfonate, 0.96 g of 6-amidino-2-naphthol methanesulfonate, 42 mg of DMAP and 1.06 g of DCC was added 5 ml of anhydrous pyridine. The resulting mixture was stirred overnight at room temperature. To the mixture was added 50 ml of acetone and the precipitate which was formed was collected by filtration. To the precipitate was added 40 ml of DMF. After stirring the precipitate which was formed was collected by filtration and 20 ml of water was added to the precipitate. The insolubles were removed by filtration. The filtrate was distilled under reduced pressure. To the residue was added 200 ml of acetone. The precipitate which was formed was collected by filtration to obtain 0.8 g of 6-amidino-2-naphthyl 4-(2-imidazolinyl)amino-benzoate dimethanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777182
Source datasetuspto-grants-1988_10
ORD IDord-1d68487e3b5c485697314b1e944ed6ec
Source noteuspto-grants-1988_10