HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isocyanate → 1-(6-Chloro-pyrido[2,3-b]pyrazin-3-yl)-3-ethyl-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | 6-Chloro-pyrido[2,3-b]pyrazin-3-ylamine | HCID 86635537 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(6-Chloro-pyrido[2,3-b]pyrazin-3-yl)-3-ethyl-urea | HCID 57947249 | 93.3% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A total of 5.0 g 6-Chloro-pyrido[2,3-b]pyrazin-3-ylamine (27.7 mmol; 1 eq) was suspended in 150 mL of dry 1,4-dioxane. 2.63 g (33.2 mmol; 1.2 eq) ethyl isocyanate was added and the reaction mixture was stirred at 100° C. for 4 hours. Additional 1.97 g (27.7 mmol; 1 eq) of ethyl isocyanate were added and the resulting solution was stirred at 100° C. for further 4 hours. After cooling to room temperature, the precipitate was filtered of and dried in vacuo to afford 6.5 g (93.3% yield) of 1-(6-Chloro-pyrido[2,3-b]pyrazin-3-yl)-3-ethyl-urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536332B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-5d1edd0bd74442209dc5845b91c37678 |
| Source note | uspto-grants-2013_09 |