Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 67111838 | HCID 67111838 | — |
| Reactant | HCID 178418785 | HCID 178418785 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67111934 | HCID 67111934 | — |
| Product | HCID 67112041 | HCID 67112041 | — |
Reaction Steps
In a reactor tube was dissolved methyl 4-imidazolecarboxylate (0.047 g, 0.37 mmol) in ethyl alcohol (2 mL). To the solution was added sodium tert-butoxide (0.035 g, 0.37 mmol) followed by 2-(4-(bromomethyl)-2-fluorophenyl)-5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine (0.081 g, 0.18 mmol) and the reaction mixture was heated to 70° C. for 1 h. The crude reaction mixture was concentrated in vacuo and purified by silica gel chromatography to afford pure ethyl 1-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzyl)-1H-imidazole-4-carboxylate and ethyl 1-(3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzyl)-1H-imidazole-5-carboxylate. MS (ESI) m/z: calculated: 498.2; Observed: 499.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842685B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-4caee61454fd4289b528a04b64825575 |
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| Source note | uspto-grants-2010_11 |
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