Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693837Generated: November 1, 2026

Iodine → N-(3-Iodopyridin-2-yl)-2,2-dimethylpropanamide

https://huagongshe.com/reaction/1693837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantSodium ThiosulfateHCID 24477—
Reactant2-(Pivaloylamino)pyridineHCID 1051519—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-Iodopyridin-2-yl)-2,2-dimethylpropanamideHCID 1094663657%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 2,2-dimethyl-N-pyridin-2-yl-propionamide (3.0 g, 17 mmol) described in Manufacturing Example 39-1-1, N,N,N′,N′-tetramethylethylenediamine (6.3 mL, 42 mmol) and tetrahydrofuran (60 mL) was added dropwise n-butyl lithium (1.6 M n-hexane solution, 30 mL, 47 mmol) at −78° C., which was stirred overnight at 0° C. Iodine (6.8 g, 27 mmol) was added to the reaction mixture at −78° C., and stirred for 1.5 hours at 0° C. Water and saturated aqueous sodium thiosulfate solution were added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=2:1) to obtain the title compound (2.9 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-0b7ddb6754534b6e82fff6cf7387a34d
Source noteuspto-grants-2012_04