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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509901Generated: October 26, 2026

Sodium Iodide → 4-[3-(3-tert-Butoxycarbonylamino-piperidin-1-yl)-propyl]-benzoic acid methyl ester

https://huagongshe.com/reaction/509901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Boc-amino)piperidineHCID 4233041—
ReactantBenzoic acid, 4-[3-[(methylsulfonyl)oxy]propyl]-, methyl esterHCID 10423370—
SolventAcetonitrileHCID 6342—
Product4-[3-(3-tert-Butoxycarbonylamino-piperidin-1-yl)-propyl]-benzoic acid methyl esterHCID 117856768—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-(3-Methanesulfonyloxy-propyl)-benzoic acid methyl ester (800 mg, 2.9 mmol), piperidin-3-yl-carbamic acid tert-butyl ester (290 mg, 1.45 mmol), potassium carbonate (500 mg, 3.6 mmol) and sodium iodide (100 mg 0.67 mmol) in acetonitrile (20 ml) are heated under reflux for two days and evaporated. The residue is taken up in dimethylsulfoxide (10 ml) and stirred at 90° C. for 5 h. The resulting mixture is purified by preparative HPLC-MS (MeOH/H2O+0.1% TFA). Potassiumcarbonate solution is added to the product, extracted with ethyl acetate, the organic phase is dried over Na2SO4 and concentrated in vacuo. LC (method F): tR=1.66 min; Mass spectrum (ESI+): m/z=377 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096548B2
Source datasetuspto-grants-2015_08
ORD IDord-28fb81251ba64e829d4d39ded25d464c
Source noteuspto-grants-2015_08