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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278235Generated: October 26, 2026

Ammonium Chloride → Tert-butyl 4-(2H-tetrazol-5-YL)piperidine-1-carboxylate

https://huagongshe.com/reaction/278235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantTert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(2H-tetrazol-5-YL)piperidine-1-carboxylateHCID 1818770160%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2.10 g (10.0 mmol) of 1-(t-butoxycarbonyl)-4-cyanopiperidine (from Step A), 1.95 g (30.0 mmol) of sodium azide and 1.60 g (30.0 mmol) of ammonium chloride in 20 mL of DMF was stirred at 100° C. for 20 h. The mixture was cooled and partitioned between 200 mL of methylene chloride and 200 mL of 1.0 N HCl and the layers were separated. The organic layer was washed with 200 mL of water, dried over magnesium sulfate and concentrated. Flash chromatography on 50 g of silica gel using 4:1 v/v methylene chloride/ethyl acetate+1% acetic acid, then 2:1 v/v methylene chloride/ethyl acetate+1% acetic acid as the eluent afforded 1.51 g (60%) of the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358979B1
Source datasetuspto-grants-2002_03
ORD IDord-204f252feebe4f45bd2e18f59a724327
Source noteuspto-grants-2002_03