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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350924Generated: November 2, 2026

Sodium Iodide → HCID 14426228, compound

https://huagongshe.com/reaction/2350924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant2-(2-chloroethyl)thiopheneHCID 11412456—
ReactantHCID 14426227HCID 14426227—
SolventAcetonitrileHCID 6342—
ProductHCID 14426228HCID 1442622881.4%

Reaction Steps

A mixture of 4-(ethyl-1,3,4-oxadiazolyl)-4-(N-phenylpropionamido)piperidine (880 mg, 2.68 mmol), 2-(2-thienyl)ethyl chloride (385 mg, 2.63 mmol), NaI (470 mg, 3.1 mmol) and Na2CO3 (2.0 g) in acetonitrile (50 ml) was refluxed for 72 hours. It was cooled down to room temperature and filtered. The filtrate was concentrated in vacuo and the residue was treated with CH2Cl2 (100 ml). The resulting mixture was filtered and the filtrate was concentrated in vacuo. The residue was chromatographed to give the product (940 mg, 2.14 mmol) as an amber oil: IR (neat) 1660 cm-1 ; NMR (60 MHz, CDCl3) δ0.88 (t, 3H, CH3CH2CO), 1.39 (t, 3H, oxadiazolyl CH3), 1.60 to 3.20 (m, 16H), 6.70 to 7.40 (m, 3H, thienyl H's) 7.44 (s, 5 H, phenyl H's). ##STR33##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871749
Source datasetuspto-grants-1989_10
ORD IDord-45b6b1f923264b7ba04f7da3e373c4f0
Source noteuspto-grants-1989_10