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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850321Generated: October 29, 2026

Guanidine Hydrochloride → HCID 178483822, compound

https://huagongshe.com/reaction/850321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 70250203HCID 70250203—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178483822HCID 178483822—

Reaction Steps

To a solution of guanidine.hydrochloride (0.4 g) in N,N-dimethylformamide (7.2 ml) was added sodium methoxide (0.76 ml, 28% in methanol) under nitrogen atmosphere. After being stirred for 15 minutes at room temperature, to the reaction mixture was added methyl 5-(2,5-dichlorophenyl)-3-[(2-dimethylaminoethyl)carbamoyl]benzoate.hydrochloride (0.36 g). After being stirred for 4 hours at room temperature, the residue was dissolved in a mixture of ethyl acetate (40 ml), tetrahydrofuran (20 ml) and water (40 ml). The aqueous layer was further extracted with a mixture of ethyl acetate (40 ml) and tetrahydrofuran (20 ml). The combined organic layer was washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was dissolved in ethanol (8 ml) and added slightly excess 4N hydrochloride in dioxane to afford [5-(2,5-dichlorophenyl)-3-[(2-dimethylaminoethyl)carbamoyl]benzoyl]guanidine.dihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017917
Source datasetuspto-grants-2000_01
ORD IDord-be9c40db16d14e61b4470bdcd7243b6d
Source noteuspto-grants-2000_01