HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715689Generated: November 2, 2026
Potassium Carbonate → N-[4-(morpholin-4-ylsulfonyl)phenyl]-4-[4-(trifluoromethyl)phenyl]-pyrimidin-2-amine
https://huagongshe.com/reaction/1715689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2E)-3-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one | HCID 5714026 | — |
| Reactant | HCID 178512580 | HCID 178512580 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | N-[4-(morpholin-4-ylsulfonyl)phenyl]-4-[4-(trifluoromethyl)phenyl]-pyrimidin-2-amine | HCID 11655630 | 75.4% |
Reaction Steps
A mixture of N-[4-(morpholin-4-ylsulfonyl)phenyl]guanidine (85 mg, 0.3 mmol), (2E)-3-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one (43 mg, 0.18 mmol), and potassium carbonate (83 mg, 0.6 mmol) in 1 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) is stirred at 105 to 110° C. for 18 hrs. It is then cooled to room temperature, and diluted with water (15 ml). The resulting suspension is filtered, and the precipitate is washed with dilute citric acid and water, and then dissolved in ethyl acetate. The organic solution is passed through a pad of silica gel, and the filtrate is evaporated. The residue is triturated with a mixture of methylene chloride and hexanes to give 63 mg of a yellow solid; mp 240-241° C.; MS (ESI) m/z 465.2 (M+H); HRMS: calcd for C21H19F3N4O3S, 464.1130; found (ESI_FT), 465.11835.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07799915B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-0b0d4f273cff466faee6c796ac61db78 |
|---|
| Source note | uspto-grants-2010_09 |
|---|