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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371506Generated: October 25, 2026

Water → 2-Pentafluoroethyl-5-fluoro-1-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1h-benzoimidazole

https://huagongshe.com/reaction/1371506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-[(3-bromopropyl)thio]-4-fluoro-HCID 14575314—
Reactant1-(Piperidin-4-yl)-5-fluoro-2-pentafluoroethyl-1 H-benzoimidazoleHCID 17989655—
SolventDimethylformamideHCID 6228—
Product2-Pentafluoroethyl-5-fluoro-1-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1h-benzoimidazoleHCID 179896568.6%

Reaction Steps

3.9 g 1-(Piperidin-4-yl)-5-fluoro-2-pentafluoroethyl-1H-benzoimidazole, 4.4 g 1-(3-bromo-propylsulfanyl)-4-fluoro-benzene and 2 g K2CO3 were stirred in 50 ml DMF at 100° C. for 2 h. After cooling the mixture was poured into water and was extracted 2× with ethyl acetate. The organic layer was tracted 3× with water, dried and evaporated. The resulting oil was purified by flash chromatography with dichloromethane, the purified fractions were dissolved in acetone after evaporation of the solvent, and the solution was acidified with etherical HCl. After evaporation of the solvent the resulting crystals were filtered with diisopropyl ether. The crystals were dissolved in acetone again and evaporated to a volume of 2 ml. The product crystallized as hydrochloride to give 0.5 g product (mp. 208–209° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157471B2
Source datasetuspto-grants-2007_01
ORD IDord-335cd671a8704912a63ee9a1a038dcb1
Source noteuspto-grants-2007_01