HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 4-{3-[(1R,5S)-3-Azabicyclo[3.1.0]hex-3-yl]propoxy}benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | (1R,5S)-3-azabicyclo[3.1.0]hexane | HCID 13150524 | — |
| Reactant | 4-(3-Chloropropoxy)benzamide | HCID 14407176 | — |
| Product | 4-{3-[(1R,5S)-3-Azabicyclo[3.1.0]hex-3-yl]propoxy}benzamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07906547B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-2c9e16f3629c4bdb92b078ff57cd55c8 |
| Source note | uspto-grants-2011_03 |