HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(2-methoxyphenethyl)imino-N-(ethylthiocarbamoyl)-5,5-dimethyl-1,3-thiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-ethyl chloromethanethioate | HCID 5325481 | — |
| Reactant | 2-(2-Methoxyphenethyl)imino-5,5-dimethyl-1,3-thiazine | HCID 22639987 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-methoxyphenethyl)imino-N-(ethylthiocarbamoyl)-5,5-dimethyl-1,3-thiazine | HCID 22639982 | 60% |
Reaction Steps
To a mixture of 2-(2-methoxyphenethyl)imino-5,5-dimethyl-1,3-thiazine (0.28 g), triethylamine (0.15 g) and dichloromethane (5 ml) was added dropwise for 3 minutes ethyl chlorothiocarbonate (0.15 g). The mixture was stirred at room temperature for 2 hours. To the solution was added water (30 ml). The mixture was extracted with diethylether (60 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to give 2-(2-methoxyphenethyl)imino-N-(ethylthiocarbamoyl)-5,5-dimethyl-1,3-thiazine (0.21 g, yield: 60%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818640B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-3ea8d6f3882347bb87c2fb1a22691ec1 |
| Source note | uspto-grants-2004_11 |