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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426228Generated: November 2, 2026

Triethylamine → N-(5-Iodopyridin-2-yl)-2,2-dimethylpropanamide

https://huagongshe.com/reaction/1426228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant2-Pyridinamine, 5-iodo-HCID 88579—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductN-(5-Iodopyridin-2-yl)-2,2-dimethylpropanamideHCID 17100900106.3%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

5-Iodopyridin-2-amine (5 g, 22.7 mmol) was dissolved in 50 ml of dichloromethane and Et3N (6.3 ml, 45.5 mmol, 2 equiv.) was added at room temperature. The mixture was cooled to 0-5° C. and pivaloyl chloride (3.4 ml, 27.3 mmol, 1.2 equiv.) was added dropwise. The reaction mixture was stirred for 1 hour at 0-5° C. Saturated NaHCO3-solution was added and the mixture was extracted with dichloromethane. The organic extracts were dried with sodium sulfate, filtered and evaporated to dryness. The desired N-(5-iodopyridin-2-yl)pivalamide (7.34 g, 99.8% yield) was obtained as a brown oil, MS: m/e=305.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933094B2
Source datasetuspto-grants-2015_01
ORD IDord-688d7ee1d15640ec83933fd26cb7c155
Source noteuspto-grants-2015_01