Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | (+-)-3-Quinuclidinol | HCID 15381 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate | HCID 10423841 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Agn-PC-00bqth | HCID 9885319 | 12.2% |
Reaction Steps
To a 30 ml toluene solution containing 0.70 g of ethyl 1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate and 0.41 g of 3-quinuclidinol, 0.03 g of sodium hydride (60%) was added. The resulting mixture was stirred at 140° C. for 2 days while removing the ethanol formed. The reaction mixture was cooled to room temperature, brine was added, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=10:1→chloroform:methanol:28% aqueous ammonia=10:1:0.1), thereby 0.11 g of 3-quinuclidinyl 1-phenyl-1,2,3,4-tetrahydro-2-isoquinolinecarboxylate was obtained as yellow oil. The resulting oil was dissolved in 10 ml of ethanol, followed by the addition of 27 mg of oxalic acid. Then, the solvent was removed under reduced pressure. The resulting solid was recrystallized from isopropanol and isopropyl ether, thereby 0.08 g of 3-quinuclidinyl 1-phenyl-1,2,3,4-tetrahydro-2-isoquinolinecarboxylate monooxalate was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174896B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-33004775a7bd49f1a7ab256e3a35bf75 |
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| Source note | uspto-grants-2001_01 |
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