HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 6-Chloro-N-(4-fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenyl)-5-methylthieno[2,3-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4,6-Dichloro-5-methylthieno[2,3-d]pyrimidine | HCID 12225263 | — |
| Reactant | 4-Fluoro-2-(oxan-4-yloxy)aniline | HCID 58413079 | — |
| Reactant | Water ammonium hydroxide | HCID 86589665 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Chloro-N-(4-fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenyl)-5-methylthieno[2,3-d]pyrimidin-4-amine | HCID 46182299 | 11.3% |
Reaction Steps
4-Fluoro-2-(tetrahydro-2H-pyran-4-yloxy)aniline (0.057 g, 0.27 mmol), 4,6-dichloro-5-methylthieno[2,3-d]pyrimidine (0.06 g, 0.27 mmol, CA56844-14-5) and para-toluene sulfonic acid (0.005 g, 0.03 mmol) were heated at 90° C. in anhydrous 1,4-dioxane (1.5 mL) for 18 hours. The solution was cooled to ambient temperature, diluted with water (2 mL) and adjusted to pH 10 (4:1 water/ammonium hydroxide solution). The precipitate was collected, washed with water and diethyl ether to yield the title compound as yellow solid (0.012 g, 11%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486953B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-4532c732f2e04d22b830ce8dc605f8e7 |
| Source note | uspto-grants-2013_07 |