Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | HCID 58505584 | HCID 58505584 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58505685 | HCID 58505685 | 65.6% |
Reaction Steps
A solution of ethyl 3-{3-[(4-bromophenyl)carbonyl]-1-(2,2-dimethylpropanoyl)-7-(pyridin-2-ylmethoxy)indolizin-2-yl}-2,2-dimethylpropanoate (225 mg, 0.363 mmol), 3-pyridyl boronic acid (89.3, 0.726 mmol), tetrakis(triphenylphosphine)palladium(0) (42.0 mg, 0.036 mmol) in THF (4.0 mL) and aqueous 20% Na2CO3 (2.0 mL) is heated at 70° C. for 24 h then cooled to 23° C. The mixture is partitioned between Et2O and water then the organics are collected, dried with MgSO4, filtered, and concentrated in vacuo. Purification of the crude by flash chromatography (SiO2, hexanes to EtOAc) gives ethyl 3-[1-(2,2-dimethylpropanoyl)-7-(pyridin-2-ylmethoxy)-3-{[4-(pyridin-3-yl)phenyl]carbonyl}indolizin-2-yl]-2,2-dimethylpropanoate (147 mg, 65%) which is dissolved in THF (1.0 mL), MeOH (1.0 mL), and 6M aqueous NaOH (0.8 mL) and heated at 50° C. for 3 h then cooled to 23° C. and acidified to pH=1 with concentrated aqueous HCl. The mixture is concentrated in vacuo, diluted with DMSO, filtered, and filtrate is purified by HPLC (25% CH3CN to 85% CH3CN in 0.1% TFA in water) to give the title compound (62 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618300B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-895d84f68c5743a89f0f2dac59cedcac |
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| Source note | uspto-grants-2013_12 |
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