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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348515Generated: October 31, 2026

Diisopropylethylamine → HCID 17836468, compound

https://huagongshe.com/reaction/348515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 9813529HCID 9813529—
ReactantHCID 17836477HCID 17836477—
SolventTolueneHCID 1140—
ProductHCID 17836468HCID 1783646817%
ProductHCID 17836475HCID 1783647510%

Reaction Conditions

Temperature100 °C

Reaction Steps

539 mg (1.44 mmol) of 4-(5-methoxybenzimidazole-2-ylthio)butanoate ethyl ester were suspended in 4 ml of toluene followed by the addition of 616 μl (3.60 mmol) of diisopropylethylamine and 384 mg (1.59 mmol) of 4-methyl-3-(bromomethyl)benzo[b]thiophene and heating at 100° C. After allowing to react overnight, saturated sodium bicarbonate solution was added followed by extraction with ethyl acetate. The organic phase was washed with water followed by drying with magnesium sulfate and concentrating the solvent under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to obtain 114 mg of 4-(1-((4-methylbenzothiophene-3-yl)methyl)-5-methoxybenzimidazole-2-ylthio)butanoate ethyl ester (yield: 17%) and 68 mg of 4-(1-((4-methylbenzothiophene-3-yl)methyl)-6-methoxybenzimidazole-2-ylthio)butanoate ethyl ester (yield: 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176320B2
Source datasetuspto-grants-2007_02
ORD IDord-486c3bfecb664a3c9241678f78ef23ab
Source noteuspto-grants-2007_02