HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921842Generated: October 31, 2026
Triacetoxyperiodinane → HCID 89922850, compound
https://huagongshe.com/reaction/921842
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | HCID 89922570 | HCID 89922570 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89922850 | HCID 89922850 | 72.8% |
Reaction Steps
2-((2-chloro-5-cyano-4-(4-hydroxybutyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (186 mg, 0.343 mmol) was taken up in DCM (3 mL) and cooled to 0° C. Dess-Martin periodinane (189 mg, 0.445 mmol) was added, and the reaction was stirred at room temperature for 1.5 h. The reaction mixture was quenched with 2M K3PO4 solution and extracted 2× with DCM. The organic layers were combined, dried over Na2SO4, filtered, and concentrated. The material was purified by flash column chromatography (0-60% EtOAc/IIex; 40 g column). 2-((2-chloro-5-cyano-4-(4-oxobutyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (135 mg) was obtained as a yellow glass.
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-2803797fb36543298f9c8eef0555bfb6 |
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| Source note | uspto-grants-2016_03 |
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