Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650526Generated: October 29, 2026

Diisopropylethylamine → N-(3-tert-butoxycarbonylaminopropyl)-4-cyano-4-(o-tolyl)piperidine

https://huagongshe.com/reaction/650526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl N-(3-bromopropyl)carbamateHCID 4460490—
Reactant4-o-Tolylpiperidine-4-carbonitrileHCID 10176570—
SolventDimethylformamideHCID 6228—
ProductN-(3-tert-butoxycarbonylaminopropyl)-4-cyano-4-(o-tolyl)piperidineHCID 21712249—

Reaction Steps

A solution of 4-cyano-4-(o-tolyl)piperidine (5.00 g, 24.9 mmol) and 1-(tert-butoxycarbonylamino)-3-bromopropane (16, 6.55 g, 27.5 mmol) in DMF (100 mL) was treated with diisopropylethylamine (4.50 mL, 25.8 mmol) at room temperature. The resulting mixture was stirred at room temperature (3 d). The solvent was removed in vacuo and the residue dissolved in dichloromethane and sodium bicarbonate solution. The aqueous layer was extracted with two additional portions of dichloromethane and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. Flash chromatography on silica gel (5% methanol/dichloromethane) afforded the title compound (25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274583B1
Source datasetuspto-grants-2001_08
ORD IDord-147422ddf5a84e54949323a0cc52a38b
Source noteuspto-grants-2001_08