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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705711Generated: October 25, 2026

Diethyl chlorophosphate → 4-[3-chloro-5-(trifluoromethyl)phenyl]-N-diethoxyphosphoryl-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine

https://huagongshe.com/reaction/705711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
ReactantSodium hydrideHCID 24758—
Reactant4-(7-Chloro-1,3-benzodioxol-5-yl)-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amineHCID 90010064—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[3-chloro-5-(trifluoromethyl)phenyl]-N-diethoxyphosphoryl-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amineHCID 7218964723%

Reaction Steps

To a mixture of 4-(7-chloro-1,3-benzodioxol-5-yl)-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine (0.766 g, 2.00 mmol) and NaH (0.054 g, 2.20 mmol) in tetrahydrofuran at 0° C. is added diethyl chlorophosphate (0.414 g, 2.40 mmol). The mixture is allowed to reach room temperature (20-25° C.) and further stirred for 12 hours. The reaction was diluted with water and extracted with ethyl acetate; the organic layer separated and further washed with water and then dried and concentrated. The residue was re-crystallized with a mixture of ethyl acetate and petrole ether to give the title compound (125 mg; 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174967B2
Source datasetuspto-grants-2015_11
ORD IDord-df0409b2864a4bf3afccdb0552921cec
Source noteuspto-grants-2015_11