Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cycloheptanol | HCID 10399 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 86721270 | HCID 86721270 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71250791 | HCID 71250791 | — |
| Product | HCID 90184510 | HCID 90184510 | — |
Reaction Steps
To a mixed solution of 2-{2-[5-(4-fluorophenyl)-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}-N-(tetrahydro-2H-pyran-4-ylmethyl)acetamide (32.0 mg, 80 μmol) and cycloheptanol (18 mg, 160 μmol) in THF (500 μL) and toluene (500 μL) were added DIAD (31.1 μL, 160 μmol) and triphenylphosphine (42.0 mg, 160 μmol), and the mixture was stirred at 80° C. for 14 hr. To the reaction mixture were added water and ethyl acetate, and the mixture was stirred for 10 min. The organic layer was filtered with Top-Phase Separation Filter Tube. The filtrate was concentrated, and the residue was purified by preparative HPLC to give a mixture (1:2, mol/mol) of a racemic title compound and racemic 2-{2-[1-cycloheptyl-3-(4-fluorophenyl)-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}-N-(tetrahydro-2H-pyran-4-ylmethyl)acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156837B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-48a90253e6cb412f88d7b407975146bc |
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| Source note | uspto-grants-2015_10 |
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