HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → N-[3-fluoro-4-(trifluoromethyl)phenyl]-5-methyl-2-(methylthio)[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-Amino-2-fluorobenzotrifluoride | HCID 2735914 | — |
| Reactant | 7-Chloro-5-methyl-2-(methylthio)-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 10512843 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[3-fluoro-4-(trifluoromethyl)phenyl]-5-methyl-2-(methylthio)[1,2,4]triazolo[1,5-a]pyrimidin-7-amine | HCID 67119856 | — |
Reaction Steps
To a suspension of 7-chloro-5-methyl-2-(methylthio)[1,2,4]triazolo[1,5-a]pyrimidine (Intermediate 8 (0.3 g, 1.397 mmol)) in ethanol (5 mL), 4-amino-2-fluorobenzotrifluoride (ALFAAESAR, 0.25 g, 1.397 mmol) was added and the mixture was stirred at room temperature for 2 h. Anhydrous ammonia (0.2 mL, 1.397 mmol) was added and solvent was removed in vacuo. The residue was purified by flash chromatography (Si, eluting with Hexane/EtOAc mixtures form 95:5 to 40:60%) to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238653B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-b206af13d4e24b5997e2449ad34b5adc |
| Source note | uspto-grants-2016_01 |