HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → HCID 68838124, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | p-Toluenesulfonyl isocyanate | HCID 77703 | — |
| Reactant | HCID 86618029 | HCID 86618029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68838124 | HCID 68838124 | — |
Reaction Steps
TosNCO (0.38 g, 1.93 mmol) was added to a solution of the product of Step 1 (0.26 g, 0.77 mmol) in DMF (2.5 mL). After stirring at room temperature for 24 h, ethylamine (3.5 mL of a 2 M solution in THF, 7 mmol) was added to the homogeneous solution, from which a solid precipitated immediately. The mixture was microwaved at 120° C. for 10 min. After cooling to 5° C. for 1 h, a precipitate was collected by filtration, washed with a small volume of MeOH and dried in vacuo at 60° C. to yield 1-ethyl-3-(5-[methyl-(1-methyl-piperidin-4-yl)-amino]-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-urea. MS m/z 409 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524860B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-7095101e63ab47bf989d936fd442f75d |
| Source note | uspto-grants-2009_04 |