HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 57228798, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | HCID 21840287 | HCID 21840287 | — |
| Product | HCID 57228798 | HCID 57228798 | 49% |
Reaction Steps
According to the same manner as that described in Example 1, (E)-3-methoxy-4-(2-phenyl-4-thiazolylmethoxy)-cinnamaldehyde was condensed with 2,4-thiazolidinedione to give 5-[3-methoxy-4-(2-phenyl-4-thiazolylmethoxy)-cinnamylidene]-2,4-thiazolidinedione (yield: 49%). This product was recrystallized from chloroform-methanol. Yellow needles, mp: 248-249° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965589 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-ccacc7f4aa6244aeb59a9d34262fdacf |
| Source note | uspto-grants-1999_10 |