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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334669Generated: October 29, 2026

2-Fluoro-6-nitrobenzaldehyde → 4-fluoro-2-(4-trimethylsilanyl-but-3-ynyl)-2H-indazole

https://huagongshe.com/reaction/334669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-6-nitrobenzaldehydeHCID 13524043—
Reactant(4-Aminobut-1-yn-1-yl)trimethylsilaneHCID 19703099—
SolventTolueneHCID 1140—
Product4-fluoro-2-(4-trimethylsilanyl-but-3-ynyl)-2H-indazoleHCID 6659836855.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-61da16cf79e24d99b283e307cb935c81
Source noteuspto-grants-2014_11