HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-6-nitrobenzaldehyde → 4-fluoro-2-(4-trimethylsilanyl-but-3-ynyl)-2H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-6-nitrobenzaldehyde | HCID 13524043 | — |
| Reactant | (4-Aminobut-1-yn-1-yl)trimethylsilane | HCID 19703099 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-fluoro-2-(4-trimethylsilanyl-but-3-ynyl)-2H-indazole | HCID 66598368 | 55.7% |
Reaction Steps
2-Fluoro-6-nitro-benzaldehyde (180 mg, 1.06 mmol) was added to a solution of 4-trimethylsilanyl-but-3-ynylamine (200 mg, 1.40 mmol) in toluene (2 mL) and the reaction mixture was stirred under reflux for 30 min in a Dean-Stark. After evaporation of the solvent, the crude product was dissolved in triethylphosphite (1 mL) and the reaction mixture was stirred at 80° C. for 4 hours. After evaporation, the crude product was purified by flash chromatography (cyclohexane/AcOEt 92.5:7.5) to yield 4-fluoro-2-(4-trimethylsilanyl-but-3-ynyl)-2H-indazole (142 mg, 0.59 mmol, 52%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883826B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-61da16cf79e24d99b283e307cb935c81 |
| Source note | uspto-grants-2014_11 |