Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cyclohexanethiol | HCID 15290 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 9-Benzyl-2-chloro-9h-purin-6-amine | HCID 276482 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 18332687 | HCID 18332687 | 86% |
Reaction Steps
To DMF suspension (10 ml) containing sodium hydride (256 mg, 6.4 mmol, 60% in mineral oil) were added cyclohexanethiol (2 ml, 16 mmol) and 6-amino-9-benzyl-2-chloropurine (100 mg, 0.39 mmol) in order. The mixture was heated at 100° C. for 3.5 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 (1% methanol/chloroform) to give the subject compound (112 mg, yield 86%).
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-8557eae6c807413d95ef90b24bee22cd |
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| Source note | uspto-grants-2001_12 |
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