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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858233Generated: October 31, 2026

Sodium Hydroxide → 5-(2,6-Difluorophenyl)aminomethyl-4-methylamino-2-methylthiopyrimidine

https://huagongshe.com/reaction/1858233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,6-DifluoroanilineHCID 79647—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant2-Methyl-4-(methylamino)pyrimidine-5-carbothialdehydeHCID 86592869—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product5-(2,6-Difluorophenyl)aminomethyl-4-methylamino-2-methylthiopyrimidineHCID 22125139236.2%

Reaction Steps

A mixture of 300 mg (1.6 mmol) of 4-methylamino-2-methylthiopyrimidine-5-carboxaldehyde, 232 mg (1.8 mmol) of 2,6-difluoroaniline and 59 mg (0.3 mmol) of 4-toluenesulfonic acid monohydrate in 30 ml of toluene was heated at reflux with azeotropic removal of water for 18 hours. The mixture was cooled and evaporated. The residue was dissolved in 20 ml of tetrahydrofuran and added dropwise to a solution of 1.6 ml (1.6 mmol) of lithium aluminium hydride (1M in tetrahydrofuran) in a further 20 ml of tetrahydrofuran. After 30 minutes the mixture was cooled in ice and 0.5 ml of water, 0.75 ml of 2M sodium hydroxide solution and finally 1 ml of water were cautiously added dropwise. The resulting suspension was filtered through a filter aid and the filtrate was evaporated. The residue was subjected to column chromatography on silica gel using diethyl ether/hexane (1:1) for the elution to yield 210 mg (44%) of 5-(2,6-difluorophenyl)aminomethyl-4-methylamino-2-methylthiopyrimidine as a white solid. [Mass spectrum (ESI) MH+ =297].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-4a4a6f5f2aef4aff9b05b9cb0b9196ab
Source noteuspto-grants-2000_11