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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293034Generated: October 30, 2026

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

https://huagongshe.com/reaction/1293034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantN-(2,2-Diphenylethyl)-2-(methylsulphonyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amineHCID 21978255—
SolventWaterHCID 962—
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 solution of N-(2,2-diphenylethyl)-2-(methylsulfonyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine (Preparation 22) (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 was heated at 120° C. for 24 hours under a nitrogen atmosphere. The mixture was cooled to room temperature and diluted with water (1000 ml) and stirring was continued for a further 1 hour. The resultant solid was filtered off and washed several times with water. The solid was then dissolved in dichloromethane and the solution was washed with water, dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The residue was azeotroped with diethyl ether (twice) to afford the title compound as an oil (17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238676B2
Source datasetuspto-grants-2007_07
ORD IDord-8f16df4103ed433ab0b5be8c7fdc750b
Source noteuspto-grants-2007_07