Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178419280 | HCID 178419280 | — |
| Reactant | HCID 178486302 | HCID 178486302 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178480440 | HCID 178480440 | 56% |
Reaction Steps
A mixture of 3 parts of poly(oxymethylene), 5 parts of 7-[(4-fluorophenyl)methyl]-8-(4-piperidinylamino)-7H-purin-6-ol dihydrobromide, 1 part of a solution of thiophene in methanol 4%, 5 parts of potassium acetate and 120 parts of methanol was hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in water and the whole was treated with sodium carbonate. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 2 parts (56%) of 7-[(4-fluorophenyl)methyl]-8-[(1-methyl-4-piperidinyl)amino] -7H-purin-6-ol; mp. 255.6° C. (compound 139).
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-123e5bee36d1496f84f5d9e814e18fd8 |
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| Source note | uspto-grants-1991_08 |
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