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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891601Generated: October 31, 2026

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

https://huagongshe.com/reaction/1891601

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 numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-47cb00b72964462bb7fa4d859568a9ad
Source noteuspto-grants-2013_08