HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415150Generated: November 1, 2026
HCID 12300651, compound → HCID 12300653, compound
https://huagongshe.com/reaction/1415150
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12300651 | HCID 12300651 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 12300653 | HCID 12300653 | — |
Reaction Steps
Thus 2,2-diphenyl-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrile described in U.S. Pat. No. 3,318,869 is reacted with sodium azide in DMF to provide 5-[1,1-diphenyl-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-1H-tetrazole. This tetrazole is reacted with ethyl chloroglyoxylate in pyridine at -6° C to provide ethyl [1,1-diphenyl-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-1,3,4-oxadiazole-2-carboxylate hydrochloride. This ester is hydrolysed in aqueous potassium hydroxide to provide 5-[1,1-diphenyl-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-1,3,4-oxadiazole-2-carboxylic acid. Heating this acid for 15 minutes in an oil bath at 130°-140° provides 5-[1,1-diphenyl-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-1,3,4-oxadiazole. The hydrochloride salt melts at 233°-234.5° C.
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-75afe263af00494392bb21dc61ed6fee |
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| Source note | uspto-grants-1977_01 |
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