HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-butyl 7-(1-phenyl-1H-tetrazol-5-yl)-2,7-diazaspiro[4.4]nonane-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Tetrazole, 5-chloro-1-phenyl- | HCID 84262 | — |
| Reactant | tert-Butyl 2,7-diazaspiro[4.4]nonane-2-carboxylate | HCID 23282813 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-butyl 7-(1-phenyl-1H-tetrazol-5-yl)-2,7-diazaspiro[4.4]nonane-2-carboxylate | HCID 71285609 | — |
Reaction Conditions
| Temperature | 115 °C |
|---|
Reaction Steps
Et3N (5 mL) was added into a solution of tert-butyl 2,7-diazaspiro[4.4]nonane-2-carboxylate (1 g) and 5-chloro-1-phenyl-1H-tetrazole (1 g) in dioxane (50 mL). The mixture was heated to 115° C. for 24 hours. The reaction was quenched with water (50 mL). The aqueous layer was extracted with EtOAc (3×50 mL). The combined organic phase was dried over MgSO4 and concentrated to give a residue which was purified by silica gel chromatography to give tert-butyl 7-(1-phenyl-1H-tetrazol-5-yl)-2,7-diazaspiro[4.4]nonane-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664213B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-9c9ca475cc9849118ddac77e2d61125e |
| Source note | uspto-grants-2014_03 |