Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473959Generated: October 31, 2026

Iodoacetamide → 2-(5-fluoro-2-(tosylimino)pyridin-1(2H)-yl)acetamide

https://huagongshe.com/reaction/1473959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
ReactantN-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamideHCID 57607460—
SolventWaterHCID 962—
Product2-(5-fluoro-2-(tosylimino)pyridin-1(2H)-yl)acetamideHCID 66991905—

Reaction Steps

Sodium hydride (0.43 g, 0.018 mol) was mixed with N,N-Dimethylformamide (67.4 mL) and N-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamide 1 (4.0 g, 0.015 mol) was added. The reaction was stirred at room temperature for 10 minutes. Iodoacetamide (3.3 g, 0.018 mol) was added and the mixture was stirred at room temperature for 24 hours. The reaction was poured into water (100 mL) and extracted with ethyl acetate (4×75 mL). Organic layers were combined then dried with magnesium sulfate and the solvent removed. The crude product was chromatographed on silica using 5% methanol in dichloromethane to give 2-(5-fluoro-2-(tosylimino)pyridin-1(2H)-yl)acetamide 2 Rf 0.26, 5% methanol.dichloromethane; MS m/z 324 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018208B2
Source datasetuspto-grants-2015_04
ORD IDord-1a281a244cf243d0859bb4568c34a28c
Source noteuspto-grants-2015_04