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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915804Generated: October 27, 2026

Caprolactam → 1-(1-methyl-4-nitro-1H-pyrazol-5-yl)azepan-2-one

https://huagongshe.com/reaction/1915804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCaprolactamHCID 7768—
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant5-bromo-1-methyl-4-nitro-1H-pyrazoleHCID 1279587—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product1-(1-methyl-4-nitro-1H-pyrazol-5-yl)azepan-2-oneHCID 8668001244.9%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of azepan-2-one (136 mg, 1.2 mmol), 5-bromo-1-methyl-4-nitro-1H-pyrazole (206 mg, 1.0 mmol), Xantphos (116 mg, 0.20 mmol) and caesium carbonate (456 mg, 1.40 mmol) in dioxane (4 mL) was degassed by bubbling nitrogen through it for 15 min. Tris(dibenzylideneacetone)dipalladium(0) (46 mg, 0.05 mmol) was then added and the mixture degassed for a further 10 min before being heated in the microwave at 140° C. for 3 hours. Water (10 mL) was added and the mixture extracted into EtOAc (3×10 mL). The combined organic layers were passed through a phase separation cartridge and concentrated under reduced pressure. The residue was purified via silica gel chromatography (0-100% EtOAc/isohexane) to give 1-(1-methyl-4-nitro-1H-pyrazol-5-yl)azepan-2-one as a brown gum (107 mg, 44%). 1H NMR (400 MHz, CDCl3) δ 8.11 (s, 1H), 3.96 (dd, J=15.2, 10.0 Hz, 1H), 3.76 (s, 3H), 3.53 (dd, J=15.2, 7.2 Hz, 1H), 2.82-2.74 (m, 2H), 2.13-1.96 (m, 3H), 1.83-1.67 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614206B2
Source datasetuspto-grants-2013_12
ORD IDord-b0e63136a3fa43bf863946388819bff1
Source noteuspto-grants-2013_12