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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927210Generated: November 1, 2026

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

https://huagongshe.com/reaction/1927210

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 1094663656.1%

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 1-2-1, N,N,N′,N′-tetramethylethylenediamine (6.3 mL, 42 mmol)), and THF (60 mL) was added n-butyl lithium (1.6 M n-hexane solution, 30 mL) by drops at −78° C., which was stirred overnight at 0° C. Iodine (6.8 g) was added at −78° C. to the reaction mixture, which was stirred for 1.5 hours at 0° C. Water and a saturated aqueous sodium thiosulfate were added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated brine, 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 titled compound (2.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183264B2
Source datasetuspto-grants-2012_05
ORD IDord-e4164981b29c4cd4a58959a02f28e5f5
Source noteuspto-grants-2012_05