Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 9-Benzyl-2-chloro-9h-purin-6-amine | HCID 276482 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 12362092 | HCID 12362092 | 73% |
Reaction Steps
To DMF suspension (10 ml) containing sodium hydride (410 mg, 10 mmol, 60% in mineral oil) were added α-toluenethiol (1.7 ml, 14 mmol) and 6-amino-9-benzyl-2-chloropurine (100 mg, 0.39 mmol) in order. The mixture was stirred under heating at 100° C. for 4.5 hours. Brine was added thereto and the mixture was extracted with ethyl acetate. The organic layer was dried on magnesium sulfate, filtrated and the solvent in the filtrate was evaporated in vacuo. The residue was purified with silica gel chromatography (0.5% methanol/chloroform) to give the subject compound (97 mg, yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329381B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-81805ae698564e1cbb20c2747b192c30 |
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| Source note | uspto-grants-2001_12 |
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