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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964954Generated: November 1, 2026

1-(2,4-Difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone → 3-(4,5-dichloropyrimidin-6-yl)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol

https://huagongshe.com/reaction/964954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,4-Difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanoneHCID 588080—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4,5-Dichloro-6-ethylpyrimidineHCID 11137668—
SolventTetrahydrofuranHCID 8028—
Product3-(4,5-dichloropyrimidin-6-yl)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-olHCID 15230633—

Reaction Steps

To a solution of LDA (13.6 mmol) in THF (50 ml) (prepared by a similar method to that used in Example 1) at -70° C. was added dropwise 4,5-dichloro-6-ethylpyrimidine (the product of part (ii)) (2.37 g, 13.3 mmol) and the resulting solution was stirred at this temperature for 10 minutes. A solution of 1-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone (2.97 g, 13.3 mmol) in THF (50 ml) was added to the reaction mixture at such a rate so as to maintain the reaction temperature below -50° C. After stirring at -70° C. for 1 hour and at -50° C. for a further 1 hour the reaction was quenched by the addition of 10% aqueous acetic acid (11 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773443
Source datasetuspto-grants-1998_06
ORD IDord-e703a5c89fcf45bca2d41d50c5b7a922
Source noteuspto-grants-1998_06