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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | HCID 14822258 | HCID 14822258 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-(4-guanidinophenyl)butanoyl]thiazolidine hydrochloride | HCID 178479369 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198450 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-5a92df905a30436689925b635f8ae8d4 |
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| Source note | uspto-grants-1993_03 |
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