HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184267Generated: October 31, 2026
Dimethylformamide → N-(2,2-diphenylethyl)-2-(methylsulphanyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine
https://huagongshe.com/reaction/2184267
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 2-Chloro-N-(2,2-diphenylethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine | HCID 10181335 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,2-diphenylethyl)-2-(methylsulphanyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine | HCID 21978277 | 99.8% |
Reaction Steps
A solution of 2-chloro-N-(2,2-diphenylethyl)-9(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine (Preparation 9) (49.7 g, 0.11 mol) and dry N,N-dimethylformamide (200 ml) was treated with sodium thiomethoxide (10 g, 0.14 mol) and the resulting mixture heated under an atmosphere of nitrogen at 100° C. for 90 minutes. The mixture was stirred at room temperature for 72 hours and heated at 100° C. for a further 2 hours. The reaction mixture was cooled and diluted with water (1000 ml). A suspension was formed which was extracted with diethyl ether (2×500 ml). The combined organic layers were washed sequentially with water and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was azeotroped with diethyl ether then pentane to afford the title compound as a foam (48.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900309B1 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-754969a09e57436fbd09ffc10a23f23c |
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| Source note | uspto-grants-2005_05 |
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