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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113515Generated: October 30, 2026

Diisopropylethylamine → (S)-2-(Quinazolin4-ylaminomethyl)-piperidine-1-carboxylic acid tert butyl ester

https://huagongshe.com/reaction/2113515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
Reactant4-ChloroquinoxalineHCID 86626011—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(Quinazolin4-ylaminomethyl)-piperidine-1-carboxylic acid tert butyl esterHCID 86593670—

Reaction Steps

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g), 4-chloroquinoxaline (0.768 g) and diisopropylethylamine (0.816 ml) were dissolved in tetrahydrofuran (75 ml) and heated to reflux for 6 hours under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with saturated sodium hydrogen carbonate solution, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 50 to 100% ethyl acetate in hexane. The title compound was obtained as a white foam (1.44 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432270B2
Source datasetuspto-grants-2008_10
ORD IDord-f013aa26b5834381bca8a1e5729c35f6
Source noteuspto-grants-2008_10