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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359616Generated: November 1, 2026

Guanidine → HCID 178464068, compound

https://huagongshe.com/reaction/1359616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidineHCID 3520—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 15388932HCID 15388932—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178464068HCID 178464068—

Reaction Steps

1.5 g of CDI are added to a suspension of 2.0 g of 6-(2-diethylaminoethoxy)-1-naphthoic acid in 50 ml of THF, and the reaction mixture is stirred at RT overnight. It is then treated with 2.0 g of guanidine, again stirred overnight and concentrated, and the residue is stirred with 100 ml of water. The precipitate formed is filtered off with suction and purified by FC using methylene chloride/methanol 1:1.0.66 g of 6-(2-diethylaminoethoxy)-1-naphthoylguanidine is obtained; m.p.: 168-169° C. 1H-NMR (DMSO-d6): δ [ppm]=1.0 (6H), 2.6 (4H), 2.85 (2H), 4.15 (2H), 7.15 (1H), 7.3 (1H), 7.4 (1H), 7.75 (2H), 8.7 (1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600072B2
Source datasetuspto-grants-2003_07
ORD IDord-afe7abf3d44b4bfe9fe7c63c02f3f4e6
Source noteuspto-grants-2003_07