HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 131725199, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | HCID 22277850 | HCID 22277850 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131725199 | HCID 131725199 | 40.2% |
Reaction Steps
To a solution of the title compound of Step B (284 mg, 0.96 mmol) in toluene (16 ml) was added 2,4-thiazolidinedione (140 mg, 1.2 mmol), a catalytic amount of piperidinium acetate which was generated from piperidine (five drops) and acetic acid (five drops) and 4 Å molecular sieves. The mixture was stirred under reflux for about four hours, cooled to room temperature, filtered and concentrated. The product was purified by preparative TLC (4% methanol in dichloromethane) to afford the title compound (153 mg). MS (APCI−) Calc: 395.0, Found: 394.0 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06960604B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-6b5aa9c73b1a404b84573df040ec3293 |
| Source note | uspto-grants-2005_11 |