HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 57186169, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | HCID 53982463 | HCID 53982463 | — |
| Product | HCID 57186169 | HCID 57186169 | 57% |
Reaction Steps
According to the same manner as that described in Example 1, 4-benzyloxy-3,5-dimethoxycinnamaldehyde was condensed with 2,4-thiazolidinedione to give 5-(4-benzyloxy-3,5-dimethoxycinnamylidene)-2,4-thiazolidinedione (yield: 57%). This product was recrystallized from chloroform-ethanol. Yellow prisms, mp: 217-218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965589 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-35fc3c939cb04192be05a733b7676516 |
| Source note | uspto-grants-1999_10 |