HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178482381, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 178482379 | HCID 178482379 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178482381 | HCID 178482381 | 75.1% |
Reaction Steps
0.6 g (1.3 mmol) trans-(4-{4-[2-(4-amino-cyclohexyl)-ethyl]-piperazin-1-yl}-5,6-dichloro-pyrimidin-2-yl)-methyl-amine trihydrochlorid was suspended in methanol. Triethylamine (0.36 ml, 2.6 mmol) was added followed by the addition potassium cyanate (0.26 g, 3.12 mmol). The mixture was refluxed for 10 hours. The solvent was removed in vacuo. The residue was triturated with water, and the precipitate was filtered to give the title compound (0.42 g 75%) MS (EI): 431.2 (MH+). 1H NMR (300 MHz, DMSO-d6 (TMS)+1 drop of cc. DCl, (ppm)): 0.91-1.12 m (2H); 1.15-1.36 m (3H); 1.56-1.92 m (6H); 2.76 s (3H); 3.00-3.21 m (4H); 3.30-3.61 m (5H); 4.15-4.31 m (2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802672B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-31f84b01b2254b03afaf947a59d705a8 |
| Source note | uspto-grants-2014_08 |