HuagongsheHuagongshe Chemistry Print Report · For research reference only
Beta-Alanine → HCID 19792088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Beta-Alanine | HCID 239 | — |
| Reactant | 3-Thiazolidineacetic acid, 4-oxo-2-thioxo- | HCID 79793 | — |
| Reactant | HCID 86746103 | HCID 86746103 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19792088 | HCID 19792088 | 57.5% |
Reaction Steps
To a room temperature solution of 1-(4-chlorobenzoyl)-5-methoxy-2 methylindole-carboxaldehyde (535 mg, 1.63 mmols) and rhodanine 3-acetic acid (345 mg, 1.80 mmols) in 15 mL of acetic acid is added β-alanine (142 mg, 1.59 mmols). The solution is heated at reflux for 1.5 hours, then allowed to cool to room temperature. Filtration, washing with acetic acid, then hexane, provides 458 mg (56%) of (Z)-5-[[1-(4 chlorobenzoyl)-5-methoxy-2-methyl-1H -indol-3-yl]methylene]-4-oxo-2-thioxo-3-thiazolidine acetic acid as a yellow solid. An analytical sample is obtained by two recrystallizations from acetonitrile: mp 204°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05143927 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-9b74fc2742404d3e8c45543131be0642 |
| Source note | uspto-grants-1992_09 |