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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268407Generated: October 31, 2026

Water → 6-((2,2-Diphenylethyl)amino)-9-(tetrahydro-2H-pyran-2-yl)-9H-purine-2-carbonitrile

https://huagongshe.com/reaction/2268407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CyanideHCID 9032—
ReactantN-(2,2-Diphenylethyl)-2-(methylsulphonyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amineHCID 21978255—
SolventDimethylformamideHCID 6228—
Product6-((2,2-Diphenylethyl)amino)-9-(tetrahydro-2H-pyran-2-yl)-9H-purine-2-carbonitrileHCID 1015939195.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

A stirred solution of N-(2,2-diphenylethyl)-2-(methylsulfonyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine (preparation 8) (20.1 g, 42.1 mmol) in dry N,N-dimethylformamide (100 ml) was treated with potassium cyanide (5.5 g, 84.6 mmol) and the mixture heated at 120° C. for 24 hr under a nitrogen atmosphere. The mixture was then cooled to room temperature, poured into water (1000 ml) and stirring continued for a further 1 hr. The resultant solid was slowly filtered and washed several times with water, then dissolved in dichloromethane. The solution washed with water, dried with anhydrous magnesium sulfate, filtered and the solvent removed under reduced pressure. The residue was then dissolved in diethyl ether and the solvent removed under reduced pressure (repeated) to afford the title compound as an oil (17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326359B1
Source datasetuspto-grants-2001_12
ORD IDord-41a728a4583142b68fb252b0fa628139
Source noteuspto-grants-2001_12