HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → S-methyl-N-[2-(2-thiazolylmethylthio)ethyl]dithiocarbamate hydriodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 2-[(Thiazol-2-yl)methylthio]ethylamine | HCID 12923403 | — |
| Product | S-methyl-N-[2-(2-thiazolylmethylthio)ethyl]dithiocarbamate hydriodide | HCID 86733689 | — |
Reaction Steps
i. 2-[(2-Aminoethyl)thiomethyl]thiazole was successively treated with carbon disulphide and methyl iodide according to the general procedure of Example 1(a)(b) to give S-methyl-N-[2-(2-thiazolylmethylthio)ethyl]dithiocarbamate hydriodide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03968227 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-e5126cc66f674b7daf123a539b4f6792 |
| Source note | uspto-grants-1976_07 |