Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 7-Chlorothieno[3,2-b]pyridine | HCID 11275251 | — |
| Reactant | HCID 57967257 | HCID 57967257 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86636115 | HCID 86636115 | 50% |
Reaction Steps
A solution of 7-chlorothieno[3,2-b]pyridine (6) (4.49 g, 26.6 mmol) in THF (20 ml) was treated with 2.5 M hexane solution of n-BuLi (11.1 mL, 27.9 mmol) at −78° C. and allowed to stir at the same temperature for 45 min. The reaction mixture was then treated with 1M ether solution of ZnCl2 (28 mL, 28 mmol) and stirred at room temperature for an additional 1 h. The reaction mixture was then treated with 56 (2.3 g, 6.7 mmol) and Pd(PPh3)4 and was heated to reflux for 2 hrs. It was quenched with saturated NaHCO3 (50 mL) and extracted with EtOAc (2×50 mL). The extract was dried over anhydrous Na2SO4, filtered and evaporated. Obtained crude product was purified by flash chromatography (using the gradient 60-80% EtOAc/hexanes as an eluent), yielding 57 (1.43 g, 50% yield). MS (m/z): 434.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907091B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-aa5f783f6f224635893d8bc2eecb0fd2 |
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| Source note | uspto-grants-2014_12 |
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