HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261256Generated: October 31, 2026
Cesium fluoride → 4-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)phenol
https://huagongshe.com/reaction/1261256
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Hydroxyphenylboronic acid | HCID 2734360 | — |
| Reactant | 2-Bromo-7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine | HCID 59424521 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)phenol | HCID 136059648 | 62.1% |
Reaction Steps
To a solution of 2-bromo-7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine (42, scheme 8) (650 mg, 1.76 mmol) in ethylene glycol dimethyl ether (18 mL) were added 4-hydroxyphenylboronic acid (486 mg, 3.52 mmol), tetrakis-triphenylphosphine palladium(0) (203 mg, 0.18 mmol), cesium fluoride (802 mg, 5.28 mmol) and a solution of sodium bicarbonate (444 mg, 5.28 mmol) in water (1 mL). The reaction mixture was purged with nitrogen, heated at 80° C. for 4 hours, quenched with saturated aqueous ammonium chloride and extracted with EtOAc. The extract was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by trituration with methanol and ether to afford title compound 153 (418 mg, 62% yield) as a yellow solid. LRMS (M+1) 383.1 (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470850B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-b3cc39a20c594b869971e7de09feabbf |
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| Source note | uspto-grants-2013_06 |
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