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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371426Generated: October 26, 2026

Pyridine → 6-Amidino-2-naphthyl 4-benzyloxycarbonylaminomethylbenzoate

https://huagongshe.com/reaction/371426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-((((Benzyloxy)carbonyl)amino)methyl)benzoic acidHCID 1479997—
ReactantHCID 13050560HCID 13050560—
SolventDiethyl EtherHCID 3283—
Product6-Amidino-2-naphthyl 4-benzyloxycarbonylaminomethylbenzoateHCID 1317688746.9%

Reaction Steps

To 50 ml of dried pyridine, were added 5.1 g of 4-benzyloxycarbonylaminomethylbenzoic acid and 4.4 g of DCC. The mixture was stirred under cooling in ice for 30 minutes, admixed with 5.0 g of 6-amidino-2-naphthol methanesulfonate and stirred for one hour under cooling in ice, then overnight at room temperature. The reaction mixture was filtered* and the filtrate was mixed with ethyl ether. The precipitate which was formed was collected by filtration and recrystallized from a DMF-ethanol mixture to obtain 3.8 g of a white powder of a white powder of 6-amidino-2-naphthyl 4-benzyloxycarbonylaminomethylbenzoate methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04532255
Source datasetuspto-grants-1985_07
ORD IDord-9e5fc2c2395f4db097b15096d444a484
Source noteuspto-grants-1985_07