HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921877Generated: October 30, 2026
Propylene Oxide → (+/-)-2-((2-Chloro-5-cyano-3-(4-(2-hydroxypropyl)-2-oxopiperazin-1-yl)phenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile
https://huagongshe.com/reaction/921877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-((2-Chloro-5-cyano-3-(2-oxopiperazin-1-yl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile | HCID 89922699 | — |
| Catalyst | Anisole | HCID 7519 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+/-)-2-((2-Chloro-5-cyano-3-(4-(2-hydroxypropyl)-2-oxopiperazin-1-yl)phenyl)amino)-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile | HCID 89923133 | 28.9% |
Reaction Steps
A suspension of 2-((2-chloro-5-cyano-3-(2-oxopiperazin-1-yl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (16 mg, 0.028 mmol) and 2-methyloxirane (8.17 mg, 0.141 mmol) in Ethanol (0.8 mL) and THF (0.2 mL) in a sealed 1-dram vial was heated at 80° C. for 6 h. LC-MS indicated completion. After concentration, purification via flash chromatography (0-10% MeOH in DCM, 12 g) gave 20 mg of the PMB protected product. This was dissolved in 1 mL of dichloroethane and then 1 drop of anisole was added followed by 0.5 mL of TFA. The solution was heated at 60° C. for 1 h. LC-MS indicated completion, and then it was cooled and concentrated. The crude was dissolved in methanol and neutralized with 7N ammonia in methanol. After stirring for 10 min it was concentrated, purification via preparative HPLC gave the title compound as a yellow solid (4.1 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-82c25872f698422a853bc06b980255b2 |
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| Source note | uspto-grants-2016_03 |
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