HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240282Generated: October 25, 2026
Water → 2-Ethyl-1-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-yl}-1H-benzimidazole
https://huagongshe.com/reaction/2240282
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 | 2-ethyl-1-(piperidin-4-yl)-1H-1,3-benzodiazole | HCID 57586032 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Ethyl-1-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-yl}-1H-benzimidazole | HCID 58599528 | 75.2% |
Reaction Steps
To a stirred solution of 1-(3-bromopropylsulfanyl)-4-fluorobenzene (0.5 g) and 2-ethyl-1-piperidin-4-yl-1H-benzimidazole (0.5 g) in DMF (5 ml) was added K2CO3 (1.0 g) and KI (0.05 g). The mixture was heated at 100° C. for 1 h, and then allowed to cool to rt. Water (50 ml) was added and the mixture extracted with ethyl acetate (80 ml), and the organic layer separated and washed with water. This was further dried and concentrated in vacuo. The oil was purified by flash chromatography (9:1 DCM:MeOH) to yield 0.6 g of the title compound as colourless crystals. Mp. 182-184° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723360B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-8292a254bd3c4f718fc793df989fc48c |
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| Source note | uspto-grants-2010_05 |
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