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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795823Generated: November 4, 2026

Dimethylformamide → N-[3,5-bis(trifluoromethyl)benzyl]-2-chloro-N-(3-hydroxypropyl)-4-iodonicotinamide

https://huagongshe.com/reaction/1795823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant3-(3,5-Bis(trifluoromethyl)benzylamino)propanolHCID 11638019—
Reactant2-Chloro-4-iodonicotinic acidHCID 17750174—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductN-[3,5-bis(trifluoromethyl)benzyl]-2-chloro-N-(3-hydroxypropyl)-4-iodonicotinamideHCID 1178636992%

Reaction Conditions

Temperature100 °C

Reaction Steps

To thionyl chloride (20 mL), 2-chloro-4-iodonicotinic acid (8.40 g) were added along with N,N-dimethylformamide (3 droplets) and the mixture was stirred at 100° C. for 3 hours. The reaction mixture was then distilled under reduced pressure to obtain a yellow residue. 3-(3,5-bis(trifluoromethyl)benzylamino)propanol (10.7 g) and triethylamine (20.6 mL) were dissolved in tetrahydrofuran (150 mL). While the mixture was chilled on an ice bath, a tetrahydrofuran solution of the yellow residue (50 mL) was added. After stirred for 1 hour, the mixture was further stirred for additional two hours at room temperature. Subsequently, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was then dried on anhydrous sodium sulfate. Following the removal of the solvent, the remaining residue was purified on a silica gel column chromatography (ethyl acetate:n-hexane=3:1) to obtain N-[3,5-bis(trifluoromethyl)benzyl]-2-chloro-N-(3-hydroxypropyl)-4-iodonicotinamide (15.4 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030107B2
Source datasetuspto-grants-2006_04
ORD IDord-13abe883f4b346bf8536000001b197bc
Source noteuspto-grants-2006_04