HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isothiocyanatoformate → 1-(6-Bromo-4-methyl-pyridin-2-yl)-3-carboethoxy-thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Reactant | 6-Bromo-4-methylpyridin-2-amine | HCID 22176507 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(6-Bromo-4-methyl-pyridin-2-yl)-3-carboethoxy-thiourea | HCID 59589729 | — |
Reaction Steps
To a solution of 6-bromo-4-methyl-pyridin-2-ylamine (0.5 g, 2.67 mmol) in dichloromethane (20 ml) cooled to 5° C. was added ethoxycarbonyl isothiocyanate (0.32 ml, 2.67 mmol) dropwise over 15 min. The reaction mixture was then allowed to warm to room temperature at which it was stirred for 16 h. Evaporation in vacuo gave a solid that was collected by filtration and thoroughly washed with cyclohexane to give the desired product. Yield 0.59 g, 69%. LCMS MI: 317.92+319.94, RT: 5.05 min, Method: 2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431596B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-5b29bc871cdc42bfb11d768ae888d4cc |
| Source note | uspto-grants-2013_04 |