Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178498281 | HCID 178498281 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178524496 | HCID 178524496 | 75.1% |
Reaction Steps
A mixture of methyl 4-({2-[7-oxo-5-({[(3-{[2-(1H-1,2,4-triazol-3-yloxy)ethyl]oxy}phenyl)methyl]amino}carbonyl)-6,7-dihydro-1H-pyrazolo[4,3-d]pyrimidin-1-yl]ethyl}oxy)benzoate obtained in Example 47 (164 mg, 0.285 mmol), 4N aqueous sodium hydroxide solution (0.250 mL), THF (2 mL), methanol (2 mL) and water (2 mL) was stirred at 90° C. for 2 hr. The solvent was evaporated under reduced pressure, and the residue was diluted with water (20 mL), and acidified with 1N hydrochloric acid (1.5 mL). The precipitated solid was collected by filtration, and washed with water (4 mL×2) and methanol (4 mL). The obtained solid was recrystallized from methanol to give the title compound as a white powder (120 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915267B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-871893bfaf1a44d6acb991b87b11926d |
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| Source note | uspto-grants-2011_03 |
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