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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265995Generated: October 26, 2026

Hydrochloric Acid → N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2-isobutoxy-6-trifluoromethyl-pyridin-3-yl)-acrylamide

https://huagongshe.com/reaction/2265995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsobutanolHCID 6560—
ReactantSodium hydrideHCID 24758—
Reactant3-(2-Chloro-6-trifluoromethyl-pyridin-3-yl)-N-(3-ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-acrylamideHCID 74382385—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2-isobutoxy-6-trifluoromethyl-pyridin-3-yl)-acrylamideHCID 7438268440%

Reaction Steps

A mixture of 3-(2-chloro-6-trifluoromethyl-pyridin-3-yl)-N-(3-ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-acrylamide (50 mg, 0.11 mmol), 2-methyl-1-propanol (20 μl, 0.22 mmol) and 60% NaH (13 mg, 0.33 mmol) in DMF was stirred at ambient temperature for 4 hrs. The reaction mixture was diluted with water and then acidified with 2N HCl solution. The aqueous phase was extracted with EtOAc and the combined organic phase was washed with brine, dried over anhydrous MgSO4 and concentrated under reduced pressure. The resulting residue was purified by column chromatography (Hex EtOAc=1/2) to give the title compound (12 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858621B2
Source datasetuspto-grants-2010_12
ORD IDord-d7248fecf35d402481ec7a69ce8521b6
Source noteuspto-grants-2010_12