HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740932Generated: October 30, 2026
Dimethyl Disulfide → HCID 13154244, compound
https://huagongshe.com/reaction/1740932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 2,2-Dimethyl-N-(4-Methyl-2-pyridyl)propionamide | HCID 3531485 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13154244 | HCID 13154244 | — |
Reaction Steps
A solution of 2-tert-butylcarbonylamino-4-picoline (Step A, 250 mg) in anhydrous ethyl ether (5 mL) was cooled to -78° C. and treated with tert-butyllithium (1.7 mL, 1.7 M), and stirred at -78° C. for 3 hrs. To this was added dimethyl disulfide (0. 177 mL) and the reaction was allowed to warm to room temperature. The mixture was diluted with water and ethyl ether. The aqueous layer was extracted with ether. The combined organic layers were washed with saturated sodium chloride, dried over sodium sulfate, and concentrated in vacuo. The resulting oil was purified by medium pressure liquid chromatography on a 21×300 mm silica column eluted with 40% ethyl acetate/methylene chloride to afford the title compound (260 mg, lower Rf spot) and 2-tert-butylcarbonylamino-4-methylthiomethylpyridine (40 mg, higher Rf spot).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05972975 |
|---|
| Source dataset | uspto-grants-1999_10 |
|---|
| ORD ID | ord-78385a36291f4b2ea9ba8c73d78299cb |
|---|
| Source note | uspto-grants-1999_10 |
|---|