Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 19785282 | HCID 19785282 | — |
| Catalyst | Mercuric oxide | HCID 30856 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 19785347 | HCID 19785347 | 14.1% |
Reaction Steps
A mixture of 15.7 parts of ethyl 4-[[[[4-(cyclopropylamino)-5-pyrimidinyl]amino]thioxomethyl]amino]-1-piperidinecarboxylate, 20 parts of mercury(II) oxide, 40 parts of ethanol and 135 parts of N,N-dimethylacetamide was stirred overnight at 80° C. The reaction mixture was filtered over diatomaceous earth while hot. The filtrate was poured into water and the product was extracted with dichloromethane. The organic layer was dried, filtered and evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 2.2 parts (14.1%) of ethyl 4-[(9-cyclopropyl-9H-purin-8-yl)amino]-1-piperidinecarboxylate; mp. 177.0° C. (compound 17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05041448 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-4d7d019a24bd449799d5156f83ca9c02 |
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| Source note | uspto-grants-1991_08 |
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