HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxy-alpha-toluenethiol → Methyl 3-[[(4-methoxyphenyl)methyl]thio]-2-pyridinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxy-alpha-toluenethiol | HCID 80407 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Reactant | methyl 3-(N,N-dimethylaminocarbamoylthio)pyridine-2-carboxylate | HCID 86742402 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-[[(4-methoxyphenyl)methyl]thio]-2-pyridinecarboxylate | HCID 14277622 | 62.2% |
Reaction Steps
A solution of 1.20 g (5 mmol) of methyl 3-(N,N-dimethylaminocarbamoylthio)pyridine-2-carboxylate in 5 mL of methanol and 1.5 mL (6 mmol) of 4.1M sodium methoxide methanol was stirred at room temperature for 10 minutes. Then the solvent was concentrated and the residue was dissolved in 5 mL of N,N-dimethylformamide and 5 mL of tetrahydrofuran. 0.936 g (6 mmol) of p-methoxybenzylmercaptan was added and the solution was stirred at room temperature for 18 hours. The solution was partitioned between ether and water and the aqueous layer was extracted with two portions of ether. The combined extracts were washed with brine, dried and concentrated. Recrystallization from methanol afforded 0.90 g (62%) of pale tan needles, m.p. 99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767766 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-08c753c85ed74497a3034fb16b17f6e1 |
| Source note | uspto-grants-1988_08 |