HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631967Generated: October 26, 2026
Water → 6-Cyclopropylmethoxy-5-(tetrahydro-pyran-4-yl)-pyridine-2-carboxylic acid
https://huagongshe.com/reaction/631967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,6-Dihydro-2H-pyran-4-boronic acid pinacol ester | HCID 11218053 | — |
| Reactant | 5-Bromo-6-cyclopropylmethoxy-pyridine-2-carboxylic acid | HCID 71087543 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Cyclopropylmethoxy-5-(tetrahydro-pyran-4-yl)-pyridine-2-carboxylic acid | HCID 71087401 | 90.9% |
Reaction Steps
Under an atmosphere of nitrogen, a solution of 5-bromo-6-(cyclopropylmethoxy)-pyridine-2-carboxylic acid (300 mg, 1.1 mmol), 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (278 mg, 1.3 mmol), 1,1′-bis(diphenylphosphino) ferrocene-palladium(II)dichloride methylene chloride complex (CAN 95464-05-4, 45 mg, 0.06 mmol) and sodium carbonate (964 mg, 9.1 mmol) in DMF (10 mL) was heated to 100° C. overnight. The reaction mixture was poured into water, extracted with ethyl acetate (30 mL), the pH of the aqueous layer was adjusted to 2 by addition of 1 N hydrochloric acid and the resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed six times with brine, dried over anhydrous sodium sulfate and evaporated. The residue was purified by column chromatography (silica gel, 8 g, 30% ethyl acetate in petroleum ether) to yield the title compound (0.15 g, 1 mmol, 49.4%) as white solid; MS (EI): m/e 276.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321727B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-47e4695318804e32bc745e27b3675514 |
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| Source note | uspto-grants-2016_04 |
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