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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | N-(2,2-Diphenylethyl)-2-(methylsulphonyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine | HCID 21978255 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-((2,2-Diphenylethyl)amino)-9-(tetrahydro-2H-pyran-2-yl)-9H-purine-2-carbonitrile | HCID 10159391 | 95.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326359B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-41a728a4583142b68fb252b0fa628139 |
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| Source note | uspto-grants-2001_12 |
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