Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Propanethiol | HCID 6364 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 9-Benzyl-2-chloro-9h-purin-6-amine | HCID 276482 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 18332807 | HCID 18332807 | 61% |
Reaction Steps
To DMF suspension (10 ml) containing sodium hydride (300 mg, 7.5 mmol 60% in mineral oil) were added 2-propanethiol (1.0 ml, 11 mmol) and 6-amino-9-benzyl-2-chloropurine (160 mg, 0.62 mmol) in order. The mixture was stirred under heating at 100° C. for 2.5 hours. Brine was added thereto and the mixture was extracted with chloroform. The organic layer was dried on magnesium sulfate, filtered 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 61%).
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-58e309e9300b499585f08531872a799a |
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| Source note | uspto-grants-2001_12 |
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