Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 76568129 | HCID 76568129 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131728296 | HCID 131728296 | — |
Reaction Steps
A mixture of racemic (2′R,3S,4′R)-6-chloro-4′-[5-chloro-2-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenyl]-2′-(2-chloro-5-fluoro-phenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione (150 mg, 0.24 mmol), NaOH (70 mg, 1.75 mmol), H2O (2 mL) and THF (6 mL) was heated at 70° C. for 1 h. After cooled to room temperature, the solution was concentrated and the residue was acidified to “pH” 2-3 by addition of concentrated aqueous HCl. The white solid was collected by filtration to give the title compound which was used for next step reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776875B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-6a37c898b4324d018bc39193bafd601b |
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| Source note | uspto-grants-2010_08 |
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