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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626978Generated: November 1, 2026

1-Methyl-4-piperidone → HCID 89810863, compound

https://huagongshe.com/reaction/626978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-piperidoneHCID 74049—
Reactant5-Bromo-2-iodopyrimidineHCID 7006651—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 89810863HCID 8981086330.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

5-Bromo-2-iodopyrimidine (2 g, 7.02 mmol) was dissolved in dry toluene (30 mL) and cooled to −78° C. under nitrogen. n-Butyllithium (2.5M solution in hexanes, 2.95 mL) was added dropwise, and the reaction mixture was stirred for 30 minutes before dropwise addition of 1-methylpiperidin-4-one (0.9 mL, 0.01 mol). The reaction mixture was stirred at −78° C. for 1 h. The reaction mixture was allowed to warm to room temperature, then diluted with 5% aqueous ammonium chloride solution (50 mL) and extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with brine (50 mL) and dried over magnesium sulphate, then the solvent removed under reduced pressure. The resulting crude material (1.55 g) was sonicated in ethyl acetate (10 mL) and DCM (1 mL), then heptane was added. The solid that formed was filtered to afford the title compound (580 mg, 29.4%) as a brown solid. LCMS Method F: MH+: m/z 272/274, RT 1.20 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309243B2
Source datasetuspto-grants-2016_04
ORD IDord-f83e72df333a40e7a14294b19305b3df
Source noteuspto-grants-2016_04