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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450585Generated: October 30, 2026

p-Toluenesulfonic acid → 6-Chloro-N-(4-fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenyl)-5-methylthieno[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/450585

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4,6-Dichloro-5-methylthieno[2,3-d]pyrimidineHCID 12225263—
Reactant4-Fluoro-2-(oxan-4-yloxy)anilineHCID 58413079—
ReactantWater ammonium hydroxideHCID 86589665—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6-Chloro-N-(4-fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenyl)-5-methylthieno[2,3-d]pyrimidin-4-amineHCID 4618229911.3%

Reaction Steps

4-Fluoro-2-(tetrahydro-2H-pyran-4-yloxy)aniline (0.057 g, 0.27 mmol), 4,6-dichloro-5-methylthieno[2,3-d]pyrimidine (0.06 g, 0.27 mmol, CA56844-14-5) and para-toluene sulfonic acid (0.005 g, 0.03 mmol) were heated at 90° C. in anhydrous 1,4-dioxane (1.5 mL) for 18 hours. The solution was cooled to ambient temperature, diluted with water (2 mL) and adjusted to pH 10 (4:1 water/ammonium hydroxide solution). The precipitate was collected, washed with water and diethyl ether to yield the title compound as yellow solid (0.012 g, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486953B2
Source datasetuspto-grants-2013_07
ORD IDord-4532c732f2e04d22b830ce8dc605f8e7
Source noteuspto-grants-2013_07