HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 5-[2-(3-Phenylureido)thiazol-4-ylmethylene]rhodanine-3-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Thiazolidineacetic acid, 4-oxo-2-thioxo- | HCID 79793 | — |
| Reactant | 2-(3-Phenylureido)thiazole-4-carbaldehyde | HCID 15053514 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[2-(3-Phenylureido)thiazol-4-ylmethylene]rhodanine-3-acetic acid | HCID 54412185 | 45.9% |
Reaction Steps
A mixture comprising 1 g of 2-(3-phenylureido)thiazole-4-carbaldehyde, 0.85 g of rhodanine-3-acetic acid, 0.76 g of piperidine and 15 ml of ethanol was stirred at room temperature for 2 hours, and the resulting mixture was left to stand overnight. The crystals which precipitated out were collected by filtration dispersed in dilute aqueous hydrochloric acid, and washed with stirring for 30 minutes. The resulting crystalline product was recrystallized from a mixture of acetic acid and ethyl acetate, giving 0.78 g of the desired compound as an orange powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933355 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-7b4ddc6af69b4c5999e9c08d89975569 |
| Source note | uspto-grants-1990_06 |