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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene OxideHCID 6378—
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-((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-carbonitrileHCID 89922699—
CatalystAnisoleHCID 7519—
SolventEthanolHCID 702—
Solvent1,1-DichloroethaneHCID 6365—
SolventTetrahydrofuranHCID 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-carbonitrileHCID 8992313328.9%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-82c25872f698422a853bc06b980255b2
Source noteuspto-grants-2016_03