HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415155Generated: October 25, 2026
Ammonium Chloride → HCID 178420261, compound
https://huagongshe.com/reaction/1415155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 2-Phenyl-(3-pyridyl)-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrile | HCID 20356966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178420261 | HCID 178420261 | — |
Reaction Steps
A mixture of 5.69 parts of 2-phenyl-(3-pyridyl)-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrile, 1.67 parts of sodium azide, 1.38 parts of ammonium chloride and 0.025 parts of lithium chloride in 30 parts by volume of dimethylformamide was stirred for 12 hours under nitrogen at 120° C. After the reaction time was completed, the material was cooled and filtered. The collected precipitate was washed with dimethylformamide and water. The precipitate was then dissolved in 100 parts by volume of 0.2N NaOH. The resultant solution was filtered. The filtrates were neutralized with dilute hydrochloric acid. The product which separated was recrystallized from ethanol. The procedure afforded 5-[1-phenyl-1-(3-pyridyl)-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-1H-tetrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04003904 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-9b8cbecba36f4c6a9d15d7ab3d618bb4 |
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| Source note | uspto-grants-1977_01 |
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