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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921333Generated: October 30, 2026

2,4-Dichloro-5-(trifluoromethyl)pyrimidine → 4-Chloro-2-[5-(dimethylphosphoryl)-3-methoxypyrazin-2-yl]-5-(trifluoromethyl)pyrimidine

https://huagongshe.com/reaction/921333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
Reactant5-(Dimethylphosphoryl)-3-methoxypyrazin-2-amineHCID 67052682—
SolventDimethylacetamideHCID 31374—
SolventDiisopropylethylamineHCID 81531—
Product4-Chloro-2-[5-(dimethylphosphoryl)-3-methoxypyrazin-2-yl]-5-(trifluoromethyl)pyrimidineHCID 86668796—

Reaction Steps

A suspension of 5-(dimethylphosphoryl)-3-methoxypyrazin-2-amine (prepared in Example 33: 2.2 mmol) in 15 mL of N,N-Dimethylacetamide and 3.6 mL of Diisopropylethylamine, is allowed to stirred at room temperature for 15 minutes until a clear solution is obtained. 2,4-Dichloro-5-(trifluoromethyl)pyrimidine (5.7 g, 2.6 mmol) is added in four portions over 5 minutes. The reaction mixture is stirred at 60 degrees for 1 hour. The reaction mixture is cooled to room temperature and filtered to obtain a white solid. The white solid is washed with 50 mL of water three times and followed by 50 mL of Ethyl ether three times. The white solid is dried under vacuum to yield 4-chloro-2-[5-(dimethylphosphoryl)-3-methoxypyrazin-2-yl]-5-(trifluoromethyl)pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273077B2
Source datasetuspto-grants-2016_03
ORD IDord-f87489d67fb34eb09f061289cf96b663
Source noteuspto-grants-2016_03