Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 86610076 | HCID 86610076 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 86610077 | HCID 86610077 | — |
Reaction Steps
To a stirred solution of phenylmethyl (2R)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-2,3-dihydro-2-methyl-1H-indole-1-carboxylate (Step 3, 2.11 g, 5.84 mmol) in water/ethanol (1:9, 60 mL) is added triethylamine (6.5 m]L, 46.7 mmol) and hydroxylamine hydrochloride (6.49 g, 93.4 mmol). The reaction mixture is stirred at 90° C. for 20 h and is then concentrated under reduced pressure. The residue is taken up in CH2Cl2 (60 mL) and washed with H2O (2×20 mL) and saline (2×20 mL), and the combined aqueous layer is extracted with CH2Cl2 (2×20 mL). The combined organic layer is dried over anhydrous sodium sulfate and concentrated under reduced pressure, and the residue is purified by chromatography on a Biotage Flash 40M 90 g silica gel cartridge (30–50% EtOAc/Hexanes eluent) to give the title compound, MS (ESI+) for C17H18N2O2 m/z 283 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141588B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-5f637438dc4d414f94e8ec62943c8be2 |
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| Source note | uspto-grants-2006_11 |
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