HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113011Generated: October 31, 2026
Potassium Carbonate → HCID 11588431, compound
https://huagongshe.com/reaction/2113011
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Isoquinoline-5-boronic acid | HCID 599474 | — |
| Reactant | Methyl 3-((4-iodophenoxy)methyl)benzoate | HCID 57643351 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11588431 | HCID 11588431 | — |
Reaction Steps
4.5 mL of a sonicated and degassed solution of 3-(4-iodo-phenoxymethyl)-benzoic acid methyl ester (of Intermediate 1; 740 mg, 2 mmol), potassium carbonate (830 mg, 6 mmol), bis(tri-cyclohexylphosphine)palladium (available from Strem Chemicals, Inc., Newburyport, Mass.; 70 mg, 0.1 mmol), dioxane (41 mL) and water (4.1 mL) was added to a reaction vial containing 5-isoquinolineboronic acid (available from Frontier Scientific, Inc., Logan, Utah; 104 mg, 0.6 mmol). The solution was sonicated and degassed. The mixture was heated in a microwave oven at 170 degrees for 25 min. The reaction mixture was filtered through silica, and washed with dioxane (1 mL) and dimethylacetamide (1 mL). 2 M potassium hydroxide solution (0.4 mL) was added. The mixture was stirred at room temperature overnight, and then 1 M HCl (0.8 mL) was added. The solvents were removed in the Genevac and then 50% aqueous methanol (2 mL) was added. The vial was centrifuged and the solvent removed. This process was repeated and then the same was dried overnight in the oven to give 3-(4-isoquinolin-5-yl-phenoxymethyl)-benzoic acid. Mass spectrum MH+=356.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524870B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-52aff32e0726492183442ad1ed69e4d5 |
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| Source note | uspto-grants-2009_04 |
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