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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214725Generated: October 30, 2026

2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-[3-(4-fluorophenyl)-propyl]-n-methoxy-acetamide → 4-Hydroxy-1-(2-morpholin-4-yl-ethyl)-5-oxo-2,5-dihydro-1h-pyrrole-3-carboxylic acid [3-(4-fluorophenyl)-propyl]-methoxy-amide

https://huagongshe.com/reaction/2214725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-[3-(4-fluorophenyl)-propyl]-n-methoxy-acetamideHCID 73855587—
Reactantparaformaldehyde N-(2-aminoethyl)morpholineHCID 86760256—
SolventMethanolHCID 887—
Product4-Hydroxy-1-(2-morpholin-4-yl-ethyl)-5-oxo-2,5-dihydro-1h-pyrrole-3-carboxylic acid [3-(4-fluorophenyl)-propyl]-methoxy-amideHCID 5470466763%

Reaction Steps

Reaction of 2-(2,2-dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-N-[3-(4-fluorophenyl)-propyl]-N-methoxy-acetamide (0.560 g, 1.66 mmol) with the paraformaldehyde-N-(2-aminoethyl)morpholine adduct in methanol using a procedure similar to the one described in the preparation of compound 13 gave 0.446 g (63% yield) of the title compound as a solid after chromatography on reversed phase silica gel. 1HNMR 400 MHz (DMSO-d6) δ (ppm); 1.84 (2H, m, CH2), 2.40 (4H, broad, 2×NCH2), 2.46 (2H, t, J=6.5 Hz, CH2), 2.56 (2H, t, J=8.1 Hz, CH2), 3.46 (2H, t, J=6.5 Hz, NCH2), 3.52 (3H, s, OCH3), 3.55 (4H, broad, 2×OCH2), 3.67 (2H, t, J=7.1 Hz, NCH2), 3.95 (2H, s, NCH2), 7.09 (2H, m, aromatics), 7.23 (2H, m, aromatics). HRMS (FAB+) calculated for C21H29FN3O5: [M+H]+: 422.209125. found: 422.208679.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109186B2
Source datasetuspto-grants-2006_09
ORD IDord-6138978201c8424a92eb494ad076eff8
Source noteuspto-grants-2006_09