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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Boc-amino)piperidine | HCID 4233041 | — |
| Reactant | Benzoic acid, 4-[3-[(methylsulfonyl)oxy]propyl]-, methyl ester | HCID 10423370 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[3-(3-tert-Butoxycarbonylamino-piperidin-1-yl)-propyl]-benzoic acid methyl ester | HCID 117856768 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096548B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-28fb81251ba64e829d4d39ded25d464c |
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| Source note | uspto-grants-2015_08 |
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