HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591250Generated: October 31, 2026
4-Amino-2-fluorobenzotrifluoride → 2-(1,1-difluoroethyl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
https://huagongshe.com/reaction/591250
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Amino-2-fluorobenzotrifluoride | HCID 2735914 | — |
| Reactant | 7-Chloro-2-(1,1-difluoroethyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 53391869 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(1,1-difluoroethyl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7-amine | HCID 51347544 | — |
Reaction Steps
A suspension of Intermediate 3 (0.1 g, 0.43 mmol) and 3-fluoro-4-(trifluoromethyl)aniline (ALFAAESAR, 0.077 g, 0.43 mmol) in ethanol (5 mL) was heated at 50° C. for 1 h. The reaction mixture was concentrated under vacuum, redissolved in DCM (20 mL) and washed with aq. Na2CO3 (2×15 mL). The organic layer was dried over anhydrous Na2SO4 filtered and concentrated under vacuum to afford a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238653B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-61e402e36509418788d37515fa7c7991 |
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| Source note | uspto-grants-2016_01 |
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