Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 86586774 | HCID 86586774 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86586775 | HCID 86586775 | — |
Reaction Steps
A mixture of (1R*,2R*,5S*,6S*)-8-benzyl-2-{[3,5-bis(trifluoromethyl)phenyl]-methoxy}-6-fluoro-6-[1-(2-methoxyethoxymethyl)-1H-tetrazol-5-yl]-1-phenyl-8-azabicyclo[3.2.1]octane (Example 172; 150 mg, 0.22 mmol), 1M solution of hydrogen chloride in ether (3 ml) and methanol (3 ml) was stirred at reflux for 9 hours. The reaction mixture was concentrated. The residue (170 mg) was treated with dichloromethane (3 ml), methanol (0.5 ml), triphenylphosphine (220 mg, 0.83 mmol) and diethyl azodicarboxylate (0.12 ml, 0.56 mmol). The reaction mixture was stirred at room temperature for 1 hour and concentrated in vacuo to give a 1:3.3 mixture of isomers A and B, respectively. Both isomers were separated by chromatography on silica gel (iso-hexane:ethyl acetate 0-20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727249B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-484a74e257504d56a745df33ad07e0af |
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| Source note | uspto-grants-2004_04 |
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