Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69198057 | HCID 69198057 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15957048 | HCID 15957048 | 35% |
Reaction Steps
To a stirring solution of rac-methyl 1-(2,4-difluorobenzyl)-3-{[(3aR*,7aS*)-1-oxooctahydro-5H-pyrrolo[3,4-c]pyridin-5-yl]methyl}-1H-pyrrolo[2,3-c]pyridine-5-carboxylate (0.09 g, 0.198 mmol) in MeOH (5 ml) was added 10% NaOH(aq) (0.5 ml, excess) and H2NOH (1 ml, excess, 50% wt. sol. in water). The resulting mixture was stirred for 16 hours at ambient temperature. The solvent was evaporated and the crude product was purified by reverse phase Prep-HPLC (20-60% acetonitrile:water) to provide the title compound as a white solid (0.032 g, 35%). 1H NMR (MeOH-d4) δ: 8.77 (s, 1H), 8.38 (s, 1H), 7.68 (s, 1H), 7.29-7.25 (m, 1H), 7.03-7.00 (m, 1H), 6.94-6.92 (m, 1H), 5.57 (s, 2H), 3.95-3.93 (m, 2H), 3.44-3.41 (m, H), 3.27-3.25 (m, 1H), 2.99-2.95 (m, 1H), 2.95-2.89 (m, 1H), 2.56-2.52 (m, 2H), 2.50-2.46 (m, 1H), 2.46-2.35 (m, H), 1.84-1.82 (m, H), 1.63-1.62 (m, H). LCMS (APCI, M+H+): 456.15. HPLC: 99% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468375B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-623544fe5500461eae74701c33288883 |
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| Source note | uspto-grants-2008_12 |
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