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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538752Generated: October 29, 2026

Sodium Iodide → HCID 56687105, compound

https://huagongshe.com/reaction/538752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67328792HCID 67328792—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 56687105HCID 56687105100%

Reaction Steps

0.200 g (1.034 mmol) of 1-methyl-4-oxopiperidine-3-carboxylate hydrochloride (commercially available, ABCR), 0.54 mL (3.102 mmol) of diisopropylethylamine, 0.155 g (1.034 mmol) of sodium iodide and 0.170 g (1.034 mmol) of 3-(chloromethyl)pyridine hydrochloride were stirred at 80° C. in 5.0 mL of anhydrous CH3CN. The reaction was monitored by HPLC and UPLC-MS. After 1 h at 80° C., the insoluble inorganic materials were filtered off and the filtrate was concentrated in vacuo to give a yellowish residue. This residue was dissolved in CH2Cl2, washed with brine, H2O, dried over Na2SO4 and concentrated in vacuo to give pure methyl 4-oxo-1-(pyridin-3-ylmethyl)piperidine-3-carboxylate (0.257 g, 1.034 mmol, quantitative yield). The product was used for the next step without further manipulation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865758B2
Source datasetuspto-grants-2014_10
ORD IDord-83c67d5dbb1240549c4daa36b872a21e
Source noteuspto-grants-2014_10