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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270314Generated: November 1, 2026

Acetaldehyde → 4-[5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazin-2-yl]-N,N-diethylaniline

https://huagongshe.com/reaction/1270314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 12095702HCID 12095702—
Product4-[5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazin-2-yl]-N,N-diethylanilineHCID 18449106—

Reaction Conditions

Temperature20 °C

Reaction Steps

10 mg (0.08 mmol) of sodium cyanoborohydride and 10 mg (0.17 mmol) of acetaldehyde are added to a solution of 40 mg (0.08 mmol) of 4-[5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazin-2-yl]aniline from example 1 in methanol and the mixture is stirred at 20° C. After expiration of the reaction time, the mixture is treated with 2N hydrochloric acid. The methanol is removed under reduced pressure and the aqueous residue is washed with dichloromethane, rendered alkaline using sodium hydroxide, and extracted twice with dichloromethane. The organic phase is dried over sodium sulfate and purified by chromatography (eluent:dichloromethane/methanol 80:1-60:1-40:1 plus a drop of NH4OH)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202243B2
Source datasetuspto-grants-2007_04
ORD IDord-4a8bde4e1b044c9fbc9d6f89afadb3f7
Source noteuspto-grants-2007_04