Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178473697 | HCID 178473697 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58118671 | HCID 58118671 | — |
Reaction Steps
To a stirred solution of O-ethyl S-[(2R)-2′-oxo-1′-{[2-(trimethylsilyl)ethoxy]methyl}-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-yl]carbonodithioate from Step B (740 mg, 1.52 mmol) in EtOH (4 mL) was added 1 N NaOH (3.0 mL, 3.0 mmol). The resulting suspension was heated at 60° C. for 90 min, then cooled and poured into H2O (50 mL). The mixture was extracted with EtOAc (2×70 mL), and the combined organic layers were washed with brine (30 mL), dried over Na2SO4, filtered, and concentrated in vacuo to yield the title compound. MS: m/z=462 (M+Na+CH3CN).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765759B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-b5c9b6502cbf43eeb693138959d837e0 |
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| Source note | uspto-grants-2014_07 |
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