Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 57985925 | HCID 57985925 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | HCID 57985885 | HCID 57985885 | 94.3% |
Reaction Steps
To a suspension of 2-[(4-methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-phenyl-methyl]-malonic acid diethyl ester (1.0 g, 2.52 mmol) in a mixture of THF/EtOH (1/1, 24 ml) was added H2O (2 ml) followed by KOH (1.41 g, 25.2 mmol). The reaction mixture was stirred at 50° C. for 4 h, and then cooled to RT and concentrated. The solid residue was dissolved in H2O. The resulting solution was cooled to 0° C. and acidified to pH 4-5 by addition of HCl (I M). The white solid precipitate was collected by filtration, washed with cold H2O and dried to afford 2-[(4-Methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-phenyl-methyl]-malonic acid (809 mg, 94% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07638517B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-d319352e808e41a79660c457f9ad0e61 |
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| Source note | uspto-grants-2009_12 |
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