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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921843Generated: October 31, 2026

Acetic Acid → HCID 89922670, compound

https://huagongshe.com/reaction/921843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-MethoxyazetidineHCID 13401996—
ReactantHCID 89922850HCID 89922850—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 89922670HCID 8992267047.8%

Reaction Steps

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 (22 mg, 0.041 mmol) was taken up in THF (0.3 mL) and a solution of 3-methoxyazetidine (5.31 mg, 0.061 mmol) in MeOH (0.1 mL) was added, followed by a drop of AcOH and sodium cyanoborohydride (5.11 mg, 0.081 mmol). The reaction was stirred at room temperature for 1 h. The reaction was diluted with EtOAc and washed with water, then brine. The organic layer was dried over Na2SO4, filtered, and concentrated. The material was purified by flash column chromatography (0-7% MeOH/DCM; 24 g column). 2-((2-chloro-5-cyano-4-(4-(3-methoxyazetidin-1-yl)butyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (12 mg) was obtained as a yellow glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-6bab8827a8f045be95d1aaa660a352db
Source noteuspto-grants-2016_03