HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361118Generated: October 30, 2026
Potassium Carbonate → 4-Bromo-1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine
https://huagongshe.com/reaction/1361118
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-[(E)-(3,5-dibromo-4-pyridinyl)methylideneamino]-4-fluoroaniline | HCID 59278325 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 4-Bromo-1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine | HCID 59278460 | — |
Reaction Steps
A mixture of N-[1-(3,5-dibromopyridin-4-yl)-meth-(E)-ylidene]-N′-(4-fluorophenyl)-hydrazine (2.0 g, 5.4 mmol), CuI (50.0 mg, 0.260 mmol), trans-N,N′-dimethylcyuclohexane-1,2-diamine (0.200 mL, 1.27 mmol), and K2CO3 (1.4 g, 0.010 mol) in NMP (10 mL) was warmed at 120° C. for 30 minutes. The reaction was monitored by HPLC-MS indicating the desired mass. The mixture was diluted with aqueous ammonium chloride (100 mL) and the resulting solid collected by filtration. The solid was dissolved in hot ethyl acetate (EtOAc), dried over magnesium sulfate, treated with activated carbon, filtered through diatomaceous earth and concentrated. The residue was passed through a pad of silica gel eluting with dichloromethane to afford 4-bromo-1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879873B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-8c73be6178ad47e59579dba6e3aeb066 |
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| Source note | uspto-grants-2011_02 |
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