Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 67278098 | HCID 67278098 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67277950 | HCID 67277950 | 36.3% |
Reaction Steps
To a solution of ethyl 4-{[(1S,2R)-2-methylcyclohexyl]amino}-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (50 mg) in tetrahydrofuran (1 mL) was added lithium aluminum hydride (21 mg) at 4° C. The reaction mixture was stirred at the same temperature for an hour, at ambient temperature for an hour, and at 60° C. for 2 hours. After cooled to ambient temperature, to the mixture was added water (0.021 ml), 15% NaOH solution (0.021 ml), water (0.063 ml) one after another. The precipitate was filtered through a celite pad. The filtrate was concentrated in vacuo. The residue was purified by preparative thin layer chromatography on silica gel eluting with chloroform:methanol=8:1 to give (4-{[(1S,2R)-2-methylcyclohexyl]amino}-1H-pyrrolo[2,3-b]pyridin-5-yl)methanol (15.6 mg) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163767B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-17c85c7170dc48909c8c5bd88e87c9af |
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| Source note | uspto-grants-2012_04 |
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