Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(3-{[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}propyl)-5-isoquinolinecarbonitrile | HCID 58149888 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178455207 | HCID 178455207 | 60.8% |
Reaction Steps
A round bottomed flask was charged with 1-(3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}propyl)-5-isoquinolinecarbonitrile (D12; 417 mg, 1.28 mmol), ethanol (10 ml), sodium bicarbonate (107 mg, 12.8 mmol) and hydroxylamine hydrochloride (710 mg, 10.2 mmol). The vessel was fitted with a reflux condenser and warmed to 65° C. overnight. The resulting slurry was diluted with ethyl acetate and filtered through celite. The filtrate was concentrated in vacuo to give a yellow oil that was purified by flash column chromatography on silica using 0% to 100% ethyl acetate in cyclohexane as eluent. The relevant fractions were pooled and concentrated in vacuo to give the title compound as a yellow solid (280 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329730B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-b6c62ab634a145ea97f9fbbc316bf646 |
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| Source note | uspto-grants-2012_12 |
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