Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | 2',3'-Dihydro-1'H-spiro[piperidine-4,4'-quinoline] | HCID 57567387 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 66675129 | HCID 66675129 | — |
Reaction Steps
KNO3 (69.97 mg, 0.69 mmol) was added portion-wise to a suspension of 1,2,3,4-tetrahydroquinolin-4-spiro-4′-piperidine (133 mg, 0.66 mmol) in 98% H2SO4 (2 mL) at 0° C. After the addition was complete, the reaction mixture was allowed to warm to room temperature and stirred for additional 2 h. The mixture was then poured into cracked ice and basified with 10% NaOH to pH 8. Boc2O (172 mg, 0.79 mmol) was added dropwise and the mixture was stirred at room temperature for 1 h. The mixture was then extracted with EtOAc and the combined organic layers were dried over Na2SO4, filtered and concentrated to yield crude 7′-nitro-spiro[piperidine-4,4′(1′H)-quinoline], 2′,3′-dihydro-carboxylic acid tert-butyl ester (230 mg), which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324242B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-03ca28be76be4f60a44e496f643d9117 |
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| Source note | uspto-grants-2012_12 |
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