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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 2-(Pivaloylamino)pyridine | HCID 1051519 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-Iodopyridin-2-yl)-2,2-dimethylpropanamide | HCID 10946636 | 56.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183264B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-e4164981b29c4cd4a58959a02f28e5f5 |
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| Source note | uspto-grants-2012_05 |
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