HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Disulfide → 2-(2-Methylthiophenyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 2-(2-Bromophenyl)imidazo[1,2-a]pyridine | HCID 2862388 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Methylthiophenyl)imidazo[1,2-a]pyridine | HCID 19866737 | — |
Reaction Steps
The product of step (a) above (546 mg) was dissolved in dry ether (10 ml) and stirred under a nitrogen atmosphere at -60°. A solution of n-butyl lithium (1.25 ml of 1.6 M) was added dropwise. After stirring for 5 minutes methyl disulphide (179 ml) was added dropwise and the mixture stirred for a further 45 minutes. The mixture was allowed to warm up to room temperature then quenched with water. The layers were separated and the aqueous layer extracted with ethyl acetate. The combined organic solution was washed with water and brine then dried and evaporated to leave the sub-title compound as a gum. MS MW 240 bp 207.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04900751 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-958596548dad4a7e90f0bd17ca0db982 |
| Source note | uspto-grants-1990_02 |