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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865915Generated: November 3, 2026

Triethylamine → 4-Chloro-6-(2,4,6-trifluorophenylamino)-2-methylsulfanyl-pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/1865915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
Reactant2,4,6-TrifluoroanilineHCID 67765—
Reactant4,6-Dichloro-2-(methylsulfanyl)pyrimidine-5-carbaldehydeHCID 4614004—
SolventChloroformHCID 6212—
Product4-Chloro-6-(2,4,6-trifluorophenylamino)-2-methylsulfanyl-pyrimidine-5-carbaldehydeHCID 5797810287%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4,6-dichloro-2-methylsulfanyl-pyrimidine-5-carbaldehyde [Santilli, et al., J. Heterocycl. Chem. 1971, 8, 445-45] (1.0 g, 4.48 mmol) in CHCl3 (20 mL) was added 2,4,6-trifluoroaniline (0.735 mg, 5 mmol) followed by Et3N (0.94 mL, 6.72 mmol, 1.5 eq). The reaction mixture turned yellow and was heated to 50° C. for 8 h, 1 M aq Na2CO3 (50 mL) was added and the layers were separated. The organic layer was washed with 50 mL satd aq NaCl solution, dried through anhydrous MgSO4 and evaporated. The crude product was purified by flash chromatography to afford 1.3 g (87%) of pure 4-chloro-6-(2,4,6-trifluorophenylamino)-2-methylsulfanyl-pyrimidine-5-carbaldehyde. LC MS (m/e)=334.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629350B2
Source datasetuspto-grants-2009_12
ORD IDord-9cd7f6bb11c94e9681dcb34eef8d265d
Source noteuspto-grants-2009_12