HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468742Generated: October 31, 2026
Potassium Carbonate → HCID 67974368, compound
https://huagongshe.com/reaction/468742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | HCID 86674935 | HCID 86674935 | — |
| Catalyst | Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) | HCID 11714597 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67974368 | HCID 67974368 | 51.1% |
Reaction Steps
A mixture of N-(7-(2-chloro-5-fluoropyridin-3-yl)isoquinolin-3-yl)cyclopropanecarboxamide (105.4 mg, 0.3084 mmol), trimethylboroxine (129.0 uL, 0.9228 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (22.3 mg, 0.0315 mmol), and potassium carbonate (112.5 mg, 0.8140 mmol) in 1,4-dioxane (2.0 mL, 26 mmol) was heated at 90° C. for 26 hours. The reaction mixture was then diluted with dichloromethane, washed with water, dried over MgSO4, filtered, and evaporated in vacuo. The crude product was purified via reverse phase HPLC and lyophilized to yield 50.6 mg (51%) of N-(7-(5-fluoro-2-methylpyridin-3-yl)isoquinolin-3-yl)cyclopropanecarboxamide. LCMS (ESI): RT (min)=3.972, M+H=322.0, method=E; 1H NMR (400 MHz, DMSO-d6) δ 10.96 (s, 1H), 9.19 (s, 1H), 8.52 (s, 2H), 8.12 (s, 1H), 7.97 (d, J=8.6 Hz, 1H), 7.86-7.67 (m, 2H), 2.47 (s, 3H), 2.08 (dd, J=12.4, 7.3 Hz, 1H), 0.86 (dd, J=9.3, 6.4 Hz, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623889B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-2da1ca01b13d416d9de212ad2714c2a7 |
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| Source note | uspto-grants-2014_01 |
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