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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602629Generated: October 26, 2026

Sodium Iodide → 4-{3-[(1R,5S)-3-Azabicyclo[3.1.0]hex-3-yl]propoxy}benzamide

https://huagongshe.com/reaction/602629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant(1R,5S)-3-azabicyclo[3.1.0]hexaneHCID 13150524—
Reactant4-(3-Chloropropoxy)benzamideHCID 14407176—
Product4-{3-[(1R,5S)-3-Azabicyclo[3.1.0]hex-3-yl]propoxy}benzamideHCID 44517826—

Reaction Steps

0.004 mole of (1R,5S)-3-azabicyclo[3.1.0]hexane and 0.002 mole of sodium iodide are added to the reaction mixture of Step 1 at ambient temperature. Refluxing is then resumed for 16 hours. The precipitate is filtered off and rinsed with acetonitrile. The filtrate is concentrated to dryness. The residue is taken up in dichloromethane. The resulting solution is extracted with sodium hydroxide solution and then with water, before being dried over magnesium sulphate and concentrated to dryness. The residue is purified by a preparative chromatography technique on a Lichroprep RP-18 phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906547B2
Source datasetuspto-grants-2011_03
ORD IDord-2c9e16f3629c4bdb92b078ff57cd55c8
Source noteuspto-grants-2011_03