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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471997Generated: October 28, 2026

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

https://huagongshe.com/reaction/1471997

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 numberUS09012462B2
Source datasetuspto-grants-2015_04
ORD IDord-37abce2efb7c4919884c679da9cca544
Source noteuspto-grants-2015_04