HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383694Generated: October 31, 2026
Thiazolidinedione → HCID 178518473, compound
https://huagongshe.com/reaction/383694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 58196405 | HCID 58196405 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178518473 | HCID 178518473 | — |
Reaction Steps
To 5-(4-chlorophenylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde (117 mg, 0.430 mmol) in EtOH was added thiazolidine-2,4-dione (50 mg, 0.430 mmol) and piperidine (43 μl, 0.430 mmol). The mixture was heated at 70° C. and the product formed quickly. The solid formed was isolated by filtration and air dried to yield 5-((5-(4-chlorophenylamino)pyrazolo[1,5-a]pyrimidin-3-yl)methylene)thiazolidine-2,4-dione. LCMS (M+1=372)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367681B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ca581cc4ed8e46688be2a4b7e5714cd6 |
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| Source note | uspto-grants-2013_02 |
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