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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740319Generated: October 31, 2026

Guanidine Hydrochloride → HCID 178505357, compound

https://huagongshe.com/reaction/1740319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantEthyl AcetateHCID 8857—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 54180626HCID 54180626—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178505357HCID 178505357—

Reaction Steps

To a solution of guanidine hydrochloride (1.54 g) in N,N-dimethylformamide (5 ml) was added sodium methoxide (2.8 ml, 28% in methanol) under nitrogen atmosphere. After being stirred for 30 minutes at room temperature, to the reaction mixture was added a solution of 2-methyl-2-trifluoromethylsulfonylaminopropyl 3-(1H-inden-3-yl)benzoate (1.01 g) in N,N-dimethylformamide (5 ml). After being stirred for 23 hours at room temperature, the reaction mixture was poured into a mixture of ethyl acetate and water. The organic layer was successively washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was purified by column chromatography on silica gel eluting with a mixture of chloroform and methanol (10:1). The eluted fractions containing the desired product were collected and evaporated in vacuo. The residue was dissolved in ethanol and crystallized from slight excess methanesulfonic acid. The crystalline was recrystallized from ethanol to give [3-(1H-inden-3-yl)benzoyl]guanidine methanesulfonate (0.22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968985
Source datasetuspto-grants-1999_10
ORD IDord-7a2ef5a546834275b933eb7246d7d86c
Source noteuspto-grants-1999_10