HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921832Generated: October 30, 2026
Trifluoroacetic acid → HCID 72710846, compound
https://huagongshe.com/reaction/921832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 89922864 | HCID 89922864 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 72710846 | HCID 72710846 | 26.6% |
Reaction Steps
2-((2-chloro-5-cyano-4-(3-hydroxypropyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (30 mg, 0.057 mmol) was taken up in DCE (0.6 mL) and anisole (0.031 mL, 0.284 mmol) was added, followed by TFA (0.175 mli, 2.268 mmol). The reaction was stirred at room temperature overnight. LCMS indicates formation of the TFA ester. The solvent was removed in vacuo and the material dissolved in 2N NH3 in MeOH. The solution was stirred at room temperature for 30 min. The solvent was removed in vacuo and the material was triturated with Et2O to remove the anisole. The material was purified by preparative HPLC to provide 2-((2-chloro-5-cyano-4-(3-hydroxypropyl)phenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (6.2 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273057B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-b49a6054ceb24159816cfa7b174d0a66 |
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| Source note | uspto-grants-2016_03 |
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