HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070884Generated: November 2, 2026
Potassium Phosphate, Tribasic → HCID 57502368, compound
https://huagongshe.com/reaction/2070884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Chloroisoquinoline-7-boronic acid | HCID 59887844 | — |
| Reactant | HCID 86640815 | HCID 86640815 | — |
| Reactant | HCID 86761641 | HCID 86761641 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57502368 | HCID 57502368 | 38.7% |
Reaction Steps
5-(1-Chloroisoquinolin-7-yl)-N-phenyl-[1,2,4]triazolo[1,5-a]pyridine-2-amine. A degassed mixture of 1-chloroisoquinolin-7-ylboronic acid (288 mg, 1.38 mmol), 5-bromo-N-phenyl-[1,2,4]triazolo[1,5-a]pyridine-2-amine (400 mg, 1.38 mmol), potassium phosphate (296 mg, 2.76 mmol) and tetrakis (triphenylphosphine)palladium(0) (160 mg, 0.138 mmol) in dimethylsulfoxide (10 mL) was heated at 90° C. under nitrogen overnight. After being cooled down to room temperature, the reaction mixture was filtered, and the filtrate was concentrated in vacuo to give the crude product, which was washed with ethyl acetate to give 541-chloroisoquinolin-7-yl)-N-phenyl-[1,2,4]triazolo[1,5-a]pyridine-2-amine (200 mg, 38.7% yield) as a solid. 1H NMR (400 MHz, DMSO-d6) δ (ppm) 9.68 (br s, 1H), 9.23 (s, 1H), 8.45 (d, J=8.4 Hz, 1H), 8.41 (d, J=5.2 Hz, 1H), 8.27 (d, J=8.8 Hz, 1H), 8.01 (d, J=5.6 Hz, 1H), 7.69 (m, 4H), 7.44 (d, J=6.0 Hz, 1H), 7.23 (t, J=7.6 Hz, 2H), 6.85 (t, J=7.2 Hz, 1H); MS (ESI) m/z: 372.1 [M+1].+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299056B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-ebf0831eef284050ae28b41dd7b2f47c |
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| Source note | uspto-grants-2012_10 |
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