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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593381Generated: October 27, 2026

Triethylamine → 2-(6-{3-[(1-Methylpiperidin-4-yloxy)-pyridin-2-ylmethyl]phenyl}hex-5-ynyl)isoindole-1,3-dione

https://huagongshe.com/reaction/593381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(5-Hexynyl)phthalimideHCID 3346053—
Reactant2-[(3-Iodophenyl)(1-methylpiperidin-4-yloxy)methyl]pyridineHCID 72694725—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(6-{3-[(1-Methylpiperidin-4-yloxy)-pyridin-2-ylmethyl]phenyl}hex-5-ynyl)isoindole-1,3-dioneHCID 86703871—

Reaction Conditions

Temperature90 °C

Reaction Steps

A screw-cap tube is charged with 2-[(3-iodophenyl)(1-methylpiperidin-4-yloxy)methyl]pyridine (105 mg, example 37), tetrakis(triphenylphosphine)palladium (52 mg), copper(I) iodide (26 mg), N-5-hexynylphthalimide (186 mg), triethylamine (400 μL) and 1-methyl-2-pyrrolidinone (4 mL). The tube is evacuated, filled with argon and sealed. After stirring at 90° C. for 14 h, the mixture is diluted with water and the aqueous phase is extracted with ethyl acetate. The pooled organic extracts are washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography over silica gel (gradient dichloromethane/methanol/ammonia from 98/2/0.5 to 95/5/0.5) to give 2-(6-{3-[(1-methylpiperidin-4-yloxy)-pyridin-2-ylmethyl]phenyl}hex-5-ynyl)isoindole-1,3-dione as an brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242959B2
Source datasetuspto-grants-2016_01
ORD IDord-13f67e5db34b494785dc05860f9d275d
Source noteuspto-grants-2016_01