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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59143Generated: October 26, 2026

1,4-Dioxane → 2-Cyclopropyl-1-(2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-yl)ethanol

https://huagongshe.com/reaction/59143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant2-(3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-6-((2,2,2-trifluoroethoxy)methyl)-pyrimidine-4-carbaldehydeHCID 117824036—
ReactantHCID 178419657HCID 178419657—
SolventTetrahydrofuranHCID 8028—
Product2-Cyclopropyl-1-(2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-yl)ethanolHCID 86344066—

Reaction Steps

2-(3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-6-((2,2,2-trifluoroethoxy)methyl)-pyrimidine-4-carbaldehyde (92 mg, 0.22 mmol) was coevaporated with dioxane and dissolved in THF (5 mL). The solution was cooled on an ice bath and (cyclopropylmethyl)magnesium bromide was added over 30 min. The mixture was quenched by addition of an ammonium chloride (aq, sat). The organic phase was separated and aquous phase was extracted with ethyl acetate (2×5 mL). The combined organic phase was dried over sodium sulfate and filtered through a short pad of silica. The solvents were removed and the residue was purified by preparative HPLC to give the title compound as a dry film 17 mg (16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439904B2
Source datasetuspto-grants-2016_09
ORD IDord-9e29fce59b4743f2b3afea152abcf297
Source noteuspto-grants-2016_09