HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846655Generated: November 3, 2026
Potassium Carbonate → HCID 67341091, compound
https://huagongshe.com/reaction/1846655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | HCID 67344271 | HCID 67344271 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67341091 | HCID 67341091 | 14.1% |
Reaction Steps
To a solution of 0.050 g (0.091 mmol) of N-{5′-bromo-4-[2-(4-methyl-[1,4]diazepan-1-yl)-2-oxo-ethyl]-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-3′-yl}-3-chloro-benzamide in N,N-dimethylformamide (3 mL) is added 0.011 g (0.091 mmol) of 3-pyridyl boronic acid followed by 0.100 g (0.725 mmol) of potassium carbonate and 0.010 g (0.009 mmol) of tetrakis(triphenylphosphine)palladium(0). The mixture is flushed with argon for 2 minutes and heated at 80° C. for 18 hours. The mixture is filtered and purified by preparative reverse phase HPLC to provide 0.007 g (14%) of the title compound (125) as a white solid. [M+H]+=547.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952004B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-00b2bd328d9d426d9963ce02b8cf189d |
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| Source note | uspto-grants-2015_02 |
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