HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775071Generated: November 2, 2026
Lithium Chloride → 3-(6-Fluoro-2-pyridinyl)-5-(3-pyridinyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazolo[3,4-c]pyridine
https://huagongshe.com/reaction/1775071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 2-Fluoro-6-(tributylstannyl)pyridine | HCID 16427115 | — |
| Reactant | HCID 71253586 | HCID 71253586 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(6-Fluoro-2-pyridinyl)-5-(3-pyridinyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazolo[3,4-c]pyridine | HCID 71254057 | 80% |
Reaction Steps
To a mixture of 3-iodo-5-(pyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[3,4-c]pyridine (GCP-P3-205-1) (200 mg, 0.44 mmol) and 2-fluoro-6-(tributylstannyl)pyridine (206 mg, 0.53 mmol) in 3 mL DMF, was added TEA 1 mL, LiCl (56 mg, 1.32 mmol) and CuI (84 mg, 0.44 mmol), and Pd(PPh3)4 (254 mg, 0.22 mmol). The reaction mixture was heated at 120° C. under microwave irradiation for 1 h, and the reaction was monitored by LCMS. Upon completion, the reaction mixture was extracted with 100 mL EtOAc, washed with 50 mL brine, and dried. The solvent was distilled off and the crude material was purified via flash chromatography, eluting with 5% to 30% ethyl acetate in heptane to afford 3-(6-fluoropyridin-2-yl)-5-(pyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[3,4-c]pyridine as a yellow solid (148 mg, 80%). ESI MS m/z=421.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260425B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-0f84ab7376ea431799c00c90f52dbb36 |
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| Source note | uspto-grants-2016_02 |
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