HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602521Generated: October 29, 2026
Potassium Carbonate → HCID 67267387, compound
https://huagongshe.com/reaction/602521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Quinoline-3-boronic acid | HCID 2734663 | — |
| Reactant | HCID 67267453 | HCID 67267453 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 67267387 | HCID 67267387 | 33.2% |
Reaction Steps
{4-[(5-Chloro-thiophen-2-ylmethyl)-amino]-2-iodophenyl}-carbamic acid ethyl ester (15 mg), 3-quinolineboronic acid (29.7 mg), palladium(II) acetate (ca. 1 mg), potassium carbonate (0.035 mL, 5M aqueous solution), and acetone (2 mL) were mixed and heated in heated in a sealed glass tube in a microwave synthesizer for 10 minutes at 125° C. After cooling to room temperature, the reaction mixture was extracted with ethyl acetate (4 mL), the organic phase washed with water (2×2 mL), and brine (2×2 mL), dried over magnesium sulfate, and filtered. The solvent was removed in vacuo, and the crude product was purified by preparative LC-MS. The collected fraction was evaporated in: vacuo, redissolved in ethyl acetate (5 mL), and the organic phase was washed with saturated aqueous sodium bicarbonate (3 mL), water (3 mL), and brine (2×2 mL). The organic phase was dried over magnesium sulfate, filtered, and the solvent was removed in vacuo to furnish the title compound (5 mg, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906537B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-bda9e553c766473b8c3c8f4acaddc944 |
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| Source note | uspto-grants-2011_03 |
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