HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pirfenidone → 2(1H)-Pyridinethione, 5-methyl-1-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pirfenidone | HCID 40632 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2(1H)-Pyridinethione, 5-methyl-1-phenyl- | HCID 11988947 | — |
Reaction Steps
1-phenyl-5-methyl-2-pyridinone (555.7 mg, 3 mmol) was reacted with Lawesson's reagent (606.7 mg, 1.5 mmol) in toluene (5 ml) at 90° C. Reaction mixture was evaporated and the target compound was isolated by column chromatography (20-30% ethyl acetate-hexane) followed by crystallization from methyl-tert-butyl ether. Yield 403 mg (67%), yellow solid. The 1H NMR spectra was consistent with the structure of Compound 18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741936B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-b4e2dcc0e8c540aa99262f8e64454dec |
| Source note | uspto-grants-2014_06 |