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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921839Generated: October 29, 2026

Acetic Acid → HCID 89923556, compound

https://huagongshe.com/reaction/921839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-MethoxyazetidineHCID 13401996—
ReactantHCID 89923126HCID 89923126—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 89923556HCID 8992355666%

Reaction Steps

2-((2-chloro-5-cyano-4-(3-oxopropyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (40 mg, 0.076 mmol) was taken up in THF (0.5 mL) and a solution of 3-methoxyazetidine (9.92 mg, 0.114 mmol) in MeOH (0.2 mL) was added, followed by a drop of AcOH and sodium cyanoborohydride (9.54 mg, 0.152 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 (0-10% MeOH/DCM; 24 g column). 2-((2-chloro-5-cyano-4-(3-(3-methoxyazetidin-1-yl)propyl)phenyl)amino)-4-(cyclopropyl(4-methoxybenzyl)amino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (30 mg) was obtained as a colorless glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-6646274bdb934380b2b8e9e73118bbef
Source noteuspto-grants-2016_03