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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374249Generated: October 25, 2026

Triethylamine → 1-{3-Fluoro-4-[4-(2-fluoro-5-nitrobenzoyl)piperazino]phenyl}-1-ethanone

https://huagongshe.com/reaction/2374249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(3-Fluoro-4-piperazin-1-ylphenyl)ethanoneHCID 685610—
Reactant2-Fluoro-5-nitrobenzoyl chlorideHCID 10976570—
Solvent1,4-DioxaneHCID 31275—
Product1-{3-Fluoro-4-[4-(2-fluoro-5-nitrobenzoyl)piperazino]phenyl}-1-ethanoneHCID 136226768%

Reaction Steps

A solution of 2-Fluoro-5-nitro-benzoyl chloride (CAS: 7304-32-7; Feng, Y.; Burgess, K.; Chem.Europ.J.; EN; 5; 11; 1999; 3261-3272) (0.054 g, 0.261 mmol) in dioxane (1 ml) was treated with triethylamine (0.073 ml, 0.522 mmol) and then with a solution of 1-(3-Fluoro-4-piperazin-1-yl-phenyl)-ethanone (CAS: 189763-57-3; WO9714690) (58 mg, 0.261 mmol) in dioxane (1 ml). The mixture was stirred at room temperature for 30 minutes. The solvent was removed in vacuo. The crude oil was taken in water. The aqueous layer was extracted 3 times with CH2Cl2. The combined extracts were dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude gum was purified on a SiO2 (Heptane/AcOEt 0%-20% (10 minutes, then 20% (5 minutes) to provide 1-{3-Fluoro-4-[4-(2-fluoro-5-nitro-benzoyl)-piperazin-1-yl]-phenyl}-ethanone (69 mg, 68%) as a light yellow solid (M+H+: 390.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462617B2
Source datasetuspto-grants-2008_12
ORD IDord-65036bf60c5b4ca8b8e253634c072d25
Source noteuspto-grants-2008_12