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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182685Generated: November 2, 2026

Triethylamine → tert-butyl 7-(1-phenyl-1H-tetrazol-5-yl)-2,7-diazaspiro[4.4]nonane-2-carboxylate

https://huagongshe.com/reaction/1182685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1H-Tetrazole, 5-chloro-1-phenyl-HCID 84262—
Reactanttert-Butyl 2,7-diazaspiro[4.4]nonane-2-carboxylateHCID 23282813—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl 7-(1-phenyl-1H-tetrazol-5-yl)-2,7-diazaspiro[4.4]nonane-2-carboxylateHCID 71285609—

Reaction Conditions

Temperature115 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664213B2
Source datasetuspto-grants-2014_03
ORD IDord-9c9ca475cc9849118ddac77e2d61125e
Source noteuspto-grants-2014_03