Iodine → N-(4-Iodopyridin-3-yl)-2,2-dimethylpropanamide

Temperature

-78 °C

The 3-(Pivaloylamino)pyridine 15 (1.9 g, 11 mmol) and tetramethylethylene-diamine (4.0 mL, 26 mmol) were dissolved in dry THF (60 mL) and cooled to −78° C. While maintaining the temperature between −78° C. and −65° C., nBuLi (2.5 M solution in hexanes, 10.6 mL, 26.5 mmol) was added dropwise. The reaction was allowed to warm to −10° C. for 2 h, and then cooled back down to −78° C. Iodine (6.73 g, 26.5 mmol) dissoved in dry THF (20 mL) was added slowly. After stirring for 2 h at −78° C., the reaction was quenched with ice. Excess iodine was destroyed with addition of saturated potassium thiosulfate solution. The product was extracted with CH2Cl2, and the organic layers were washed with brine. The mixture was concentrated in vacuo to a black oil which was chromatographed (1:1 EtOAc/Hexanes; 2:1 EtOAc/Hexanes) to give 700 mg (23%) of 2,2-dimethyl-N-(4-iodo-3-pyridinyl)propanamide as a yellow solid. 1HNMR (DMSO-d6 300 MHz) δ 9.24 (s, 1H), 8.35 (s, 1H), 8.04 (d, 1H), 7.95 (d, 1H), 1.26 (s, 9H). MS (ES+)=305.

1. additionwas added dropwise
2. temperatureto warm to −10° C. for 2 h
3. temperaturecooled back down to −78° C
4. additionwas added slowly
5. customthe reaction was quenched with ice
6. customExcess iodine was destroyed with addition of saturated potassium thiosulfate solution
7. extractionThe product was extracted with CH2Cl2
8. washthe organic layers were washed with brine
9. concentrationThe mixture was concentrated in vacuo to a black oil which
10. customwas chromatographed (1:1 EtOAc/Hexanes; 2:1 EtOAc/Hexanes)

ORD record

ord-5120f793130749caad3423942244f529

Source dataset

uspto-grants-2005_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06887996B2