Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 86602412 | HCID 86602412 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69182107 | HCID 69182107 | — |
Reaction Steps
To a mixture of ethyl 3-[1-ethyl-6-formyl-4-(5-methyl-3-pyridyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]propanoate (30 mg), morpholine (36 μl) and AcOH (0.1 ml) in EtOH (1 ml) was added sodium cyanoborohydride (15 mg) at room temperature and stirred at room temperature for 5 hours. The reaction mixture was acidified to pH 3 with HCl and stirred for 30 minutes. The solution was neutralized with aqueous NaOH and extracted with EtOAc (×3). The organic layer was combined, washed with brine and dried over MgSO4. The solvent was removed under reduced pressure. The residue was purified by flash column chromatography on silica gel(CHCl3-MeOH 97:3) to give ethyl 3-[1-ethyl-4-(5-methyl-3-pyridyl)-6-(4-morpholinylmethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]propanoate (35 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459451B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-9f9a7057bc60451eab5eb1c88f41be5f |
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| Source note | uspto-grants-2008_12 |
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