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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876842Generated: November 2, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → tert-butyl 4-(3-cyano-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1876842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
ReactantTert-butyl 4-(3-cyanoprop-2-en-1-yl)piperidine-1-carboxylateHCID 67155885—
SolventAcetonitrileHCID 6342—
Producttert-butyl 4-(3-cyano-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propyl)piperidine-1-carboxylateHCID 6875394880.1%

Reaction Steps

To a solution of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.28 g, 6.60 mmol) in acetonitrile (33.0 mL) was added tert-butyl 4-(3-cyanoprop-2-en-1-yl)piperidine-1-carboxylate (3.30 g, 13.2 mmol), followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (0.987 mL, 6.60 mmol). The resulting mixture was stirred at room temperature overnight. After evaporating the reaction mixture to dryness, the residue was purified on silica gel, eluting with 0-50% EtOAc in hexanes, to give the desired product (2.35 g, 80%). LCMS (M+H) 445.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309718B2
Source datasetuspto-grants-2012_11
ORD IDord-46b2a271547240149fc63690b97007de
Source noteuspto-grants-2012_11