Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466015Generated: October 31, 2026

Ozone → tert-Butyl 4-(6-cyano-1,2,3,4-tetrahydronaphthalen-2-yl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1466015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-Boc-allylglycine methyl esterHCID 22243128—
Reactant6-Amino-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 51358340—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(6-cyano-1,2,3,4-tetrahydronaphthalen-2-yl)-3-oxopiperazine-1-carboxylateHCID 131732668—

Reaction Steps

Ozone was bubbled into a solution of methyl [allyl(tert-butoxycarbonyl)amino]acetate (3.6 g, 16 mmol) in DCM at −78° C. until it turned pale blue. Nitrogen was then bubbled into the solution to remove excess ozone. When the blue color was gone, 6-amino-5,6,7,8-tetrahydronaphthalene-2-carbonitrile (2.7 g, 16 mmol) and sodium triacetoxyborohydride (20 g, 95 mmol) was added to the reaction, and the mixture was allowed to warm to RT. The reaction was diluted with DCM, washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate, and purified by preparative TLC to afford the title compound. LC-MS (IE, m/z): 256 [M−Boc+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-0c62d7bb25aa4a75838b4dd9807c69cb
Source noteuspto-grants-2015_04