HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503118Generated: October 30, 2026
Tributylphenyltin → 3-Phenyl-1H-5-indazolecarbonitrile
https://huagongshe.com/reaction/503118
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylphenyltin | HCID 607632 | — |
| Reactant | tert-Butyl 3-bromo-5-cyano-1H-indazole-1-carboxylate | HCID 22260825 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Phenyl-1H-5-indazolecarbonitrile | HCID 13066956 | 57.3% |
Reaction Steps
To a solution of 300 mg of tert-butyl 3-bromo-5-cyano-1H-1-indazolecarboxylate produced in Production Example I-14-b in 10 ml dimethylformamide were added 376 mg of tri-n-butyl(phenyl)tin and 54 mg of tetrakis(triphenylphosphine)palladium(0), and the mixture was stirred at 150° C. for 45 minutes. After removing the solvent by distillation, the residue was dissolved in 1.5 ml of ethyl acetate and the mixture was adsorbed by 1.5 g of silica gel. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:toluene=3:97 to 1:19) and the resulting amorphous powder was crystallized from diisopropyl ether, to give 117 mg of the title compound as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776890B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-ebec3da8230a4b85932f23ec421b8491 |
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| Source note | uspto-grants-2010_08 |
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