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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 1-[(3-bromopropyl)thio]-4-fluoro- | HCID 14575314 | — |
| Reactant | 1-(Piperidin-4-yl)-5-fluoro-2-pentafluoroethyl-1 H-benzoimidazole | HCID 17989655 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Pentafluoroethyl-5-fluoro-1-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1h-benzoimidazole | HCID 17989656 | 8.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157471B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-335cd671a8704912a63ee9a1a038dcb1 |
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| Source note | uspto-grants-2007_01 |
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