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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280552Generated: October 29, 2026

p-Toluenesulfonic acid → HCID 18425436, compound

https://huagongshe.com/reaction/1280552

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,6-DichloroanilineHCID 11846—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Methyl-4-(methylamino)pyrimidine-5-carbothialdehydeHCID 86592869—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 18425436HCID 18425436298%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 4-methylamino-2-methylthiopyrimidine-5-carboxaldehyde (6 g, 32.8 mmol), 2,6-dichloroaniline (5.5 g, 33.9 mmol) and 4-toluene-sulfonic acid (1 g, 5.3 mmol) in 70 mL of toluene was heated under reflux with azeotropic removal of water for 17 hours. The mixture was concentrated to a volume of about 10 mL under reduced pressure and then treated with 120 mL of ethanol. The suspension obtained was heated to 75° C. and treated over a period of 15 minutes with 6.2 g (160 mmol) of sodium borohydride pellets. The mixture was stirred for a further 15 minutes and cooled to room temperature. The solvent was evaporated under reduced pressure and the residue was stirred in a mixture of 200 mL of 2M sodium hydroxide solution and 200 mL of ethyl acetate for 1 hour. The phases were separated and the organic phase was dried over magnesium sulfate and filtered. Evaporation of the filtrate under reduced pressure and flash chromatography of the residue using 3:7 diethyl ether/hexane for the elution gave 5.2 g (48%) of 5-(2,6-dichlorophenyl)aminomethyl-4-methylamino-2-methylthio-pyrimidine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451804B1
Source datasetuspto-grants-2002_09
ORD IDord-af3f1183d80e4ac0801c178266ad1aaa
Source noteuspto-grants-2002_09