Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | p-Chlorophenethylic alcohol | HCID 74647 | — |
| Reactant | HCID 86647566 | HCID 86647566 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66630814 | HCID 66630814 | — |
Reaction Steps
The title compound is prepared by adding N-{(3aR,4S,6R,6aS)-6-[2-Chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-yl}-propionamide (example 235, step 1) to a premixed solution of sodium hydride (60% in oil) and 2-(4-chloro-phenyl)-ethanol (1 equivalent) in dry THF. The reaction is stirred at 50° C. for 48 hours, before quenching residual sodium hydride with excess aqueous ammonium chloride. The reaction mixture id then partitioned between ethyl acetate and water; the organic phase is washed consecutively with water and brine before drying over magnesium sulfate. Filtration and removal of the volatile components under reduced pressure yields the crude product; purification by column chromatography/crystallisation affords the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258141B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-959e549406b04c8694c19bafea170953 |
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| Source note | uspto-grants-2012_09 |
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