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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920198Generated: October 30, 2026

Diisopropylethylamine → Diethyl 4-methyl-1-(3-nitropyridin-4-yl)piperidin-3-ylphosphoramidate

https://huagongshe.com/reaction/1920198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
ReactantHCID 67045186HCID 67045186—
SolventIsopropanolHCID 3776—
ProductDiethyl 4-methyl-1-(3-nitropyridin-4-yl)piperidin-3-ylphosphoramidateHCID 6750037152%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of diethyl 4-methylpiperidin-3-ylphosphoramidate (1.0 equiv.) in isopropyl alcohol was added 4-chloro-3-nitropyridine (2.0 equiv.) and DIEA (1.1 equiv.). The reaction was heated to 70° C. for 18 h, then quenched with water and extracted with ethyl acetate. The organics were dried and concentrated under vacuo. The crude was purified via ISCO (ethyl acetate and hexanes) to yield diethyl 4-methyl-1-(3-nitropyridin-4-yl)piperidin-3-ylphosphoramidate in 52% yield. LCMS (m/z): 373.0 (MH+), Rt=1.93 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168794B2
Source datasetuspto-grants-2012_05
ORD IDord-9fad0691074c491980ccb0a3e3808a0c
Source noteuspto-grants-2012_05