Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 23120475 | HCID 23120475 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 57798921 | HCID 57798921 | 90.3% |
Reaction Steps
1,4-Dioxa-8-aza-spiro[4.5]decan-8-carboxylic acid(4-{[2-(2-methyl-2H-indazol-6-ylcarbamoyl)-phenylamino]-methyl}-pyridin-2-yl)-amide (564 mg, 1.04 mmol) in acetone (35 mL), was cooled to 4° C. and treated dropwise with aqueous hydrochloric acid (4 N, 9 mL). The reaction was warmed to rt and stirred overnight. The reaction was made basic by the addition of saturated aqueous sodium hydrogencarbonate and extracted with EtOAc. The organic phase was washed with brine, dried, filtered and concentrated in vacuo to give 4-oxo-piperidine-1-carboxylic acid (4-{[2-(2-methyl-2H-indazol-6-ylcarbamoyl)-phenylamino]-methyl}-pyridin-2-yl)-amide (467 mg, 90%) as a solid; 1H-NMR (300 MHz, d6-DMSO) 10.14 (1H, s), 9.36 (1H, s), 8.25 (1H, s), 8.17 (1H, d), 8.10 (1H, s), 7.96 (1H, t), 7.86 (1H, s), 7.72 (1H, d), 7.64 (1H, d), 7.23-7.32 (2H, m), 6.96-6.98 (1H, m), 6.66 (1H, t), 6.55 (1H, d), 4.45 (2H, d), 4.13 (3H, s), 3.72-3.76 (4H, m), 2.36-2.40 (4H, m); m/z (ES+) 498 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572794B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-d897f506d5e5455f9d158a9e66142fec |
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| Source note | uspto-grants-2009_08 |
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