Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propyl mercaptan | HCID 7848 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59516128 | HCID 59516128 | — |
| Solvent | Butyronitrile | HCID 8008 | — |
| Product | HCID 59516103 | HCID 59516103 | — |
Reaction Steps
tert-butyl 5-chloro-1-[4-(methoxycarbonylmethyl)phenyl]pyrazole-4-carboxylate (Intermediate#37) (767 mg, 2.19 mmol) was dissolved in butyronitrile (10 mL). Potassium carbonate (906 mg, 6.57 mmol) and propanethiol (284 μL, 2.74 mmol) were added and the mixture heated at 90° C. for 18 h. The reaction mixture was cooled to ambient and ethyl acetate (50 mL) was added. The mixture was washed with water (4×25 mL), dried (MgSO4) and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (elution gradient 0-25% EtOAc in isohexane) to afford tert-butyl 1-[4-(methoxycarbonylmethyl)phenyl]-5-propylsulfanyl-pyrazole-4-carboxylate as a yellow oil. (527 mg, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07816391B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-ce744b62dc734808bf7e21bca7dffa46 |
|---|
| Source note | uspto-grants-2010_10 |
|---|