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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796455Generated: October 26, 2026

Ethyl 3-aminopropanoate → Ethyl 3-{4-[(diethylamino)carbonyl]-2-nitroanilino}propanoate

https://huagongshe.com/reaction/1796455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-aminopropanoateHCID 419889—
ReactantN,N-diethyl-4-fluoro-3-nitrobenzamideHCID 22181444—
SolventEthanolHCID 702—
ProductEthyl 3-{4-[(diethylamino)carbonyl]-2-nitroanilino}propanoateHCID 2218135563.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

Following general procedure 2B: A mixture of N,N-diethyl-4-fluoro-3-nitrobenzamide (0.200 g, 0.833 mmol), ethyl 3-aminopropanoate (0.116 g, 0.757 mmol) in 80% aq. EtOH (5 mL) was heated at 90° C. overnight. After work-up, the crude product was purified by silica gel column chromatography (50% EtOAc/Hexanes to 100% EtOAc) to provide the title compound (0.162 g, 63%). 1H-NMR (CDCl3): δ 8.34 (br t, J=5.6 Hz, 1H), 8.29 (d, J=2.0 Hz, 1H), 7.58 (dd, J=8.4 Hz, J=2.0 Hz, 1H), 6.92 (d, J=9.2 Hz, 1H), 4.21 (q, J=7.2 Hz, 2H), 3.69 (q, J=6.4 Hz, 2H), 3.44 (br s, 4H), 2.72 (t, J=6.4 Hz, 2H), 1.30 (t, J=6.4 Hz, 3H), 1.22 (t, J=6.8 Hz, 6H). MS (ESI) (M+H)+=338.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030139B2
Source datasetuspto-grants-2006_04
ORD IDord-3d6d43b96a0a4a26b81248ba0329f890
Source noteuspto-grants-2006_04