Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 2-Cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine | HCID 89690398 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89690439 | HCID 89690439 | — |
Reaction Steps
To a solution of 2-cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine (742 mg) in THF (25 ml) was added n-butyllithium (1.6 M in hexane, 6.2 ml) at −78° C. The mixture was stirred at −78° C. under N2 atmosphere for 30 min. After being stirred, boric acid triisopropyl ester (0.86 ml) was added to the reaction mixture at −78° C. The mixture was stirred at −78° C. under N2 atmosphere for 30 min and then at room temperature for 3 h. The mixture was poured into 1 M NaOH at 0° C. and washed with EtOAc. The aqueous layer was neutralized with 1 M HCl (to pH 7.0) and extracted with EtOAc/IPA. The organic layer was separated, washed with brine, dried over MgSO4 and concentrated in vacuo. The resulting solid was washed with EtOAc/MeOH to give the title compound (176 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365540B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-976cdd4e408f475e9e7cd981177fcce4 |
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| Source note | uspto-grants-2016_06 |
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