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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614563Generated: November 1, 2026

Cyanamide → N-[4-(4-guanidinophenyl)butanoyl]thiazolidine hydrochloride

https://huagongshe.com/reaction/1614563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantHCID 14822258HCID 14822258—
SolventEthanolHCID 702—
ProductN-[4-(4-guanidinophenyl)butanoyl]thiazolidine hydrochlorideHCID 17847936964%

Reaction Conditions

Temperature70 °C

Reaction Steps

1 mmol of N-[4-(4-aminophenyl)butanoyl]thiazolidine hydrochloride prepared in Example 20 and 1 mmol of cyanamide were dissolved with 5 ml of anhydrous ethanol. The solution was stirred under heating at 70° C. for 4 hours. The reaction mixture was concentrated under reduced pressure to obtain a crystalline residue, which was recrystallized from an ethanol-ether mixed solvent to obtain 210 mg of colorless crystals of N-[4-(4-guanidinophenyl)butanoyl]thiazolidine hydrochloride (yield: 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198450
Source datasetuspto-grants-1993_03
ORD IDord-5a92df905a30436689925b635f8ae8d4
Source noteuspto-grants-1993_03