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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240283Generated: October 30, 2026

Water → 2-Butyl-1-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-yl}-1H-benzimidazole

https://huagongshe.com/reaction/2240283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-[(3-bromopropyl)thio]-4-fluoro-HCID 14575314—
Reactant2-butyl-1-piperidin-4-yl-1H-benzimidazoleHCID 68584942—
SolventDimethylformamideHCID 6228—
Product2-Butyl-1-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-yl}-1H-benzimidazoleHCID 5859952287.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 1-(3-bromopropylsulfanyl)-4-fluorobenzene (0.2 g) and 2-butyl-1-piperidin-4-yl-1H-benzimidazole (0.3 g) in DMF (5 ml) was added K2CO3 (0.6 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 0.3 g of the title compound as colourless crystals. Mp. 159-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723360B2
Source datasetuspto-grants-2010_05
ORD IDord-6c4e720a98f64b2d8cc2ebda8462f62d
Source noteuspto-grants-2010_05