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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354203Generated: November 2, 2026

Citric Acid → N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-[(2-methylprop-2-en-1-yl)oxy]-2-nitrobenzamide

https://huagongshe.com/reaction/2354203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant2-Buten-1-olHCID 20024—
ReactantSodium hydrideHCID 24758—
Reactant5-fluoro-N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-2-nitrobenzamideHCID 66918974—
SolventDimethylacetamideHCID 31374—
ProductN-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-[(2-methylprop-2-en-1-yl)oxy]-2-nitrobenzamideHCID 66918925—

Reaction Steps

To a solution of methylallyl alcohol (3.6 ml) in anhydrous DMA (200 ml) was added sodium hydride (60% dispersion in oil, 6.7 g) and the solution stirred for 1 hour. N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-fluoro-2-nitrobenzamide (10 g) was added and the mixture stirred at room temperature for 18 hours. The mixture was poured into 1N citric acid (300 ml) and the precipitated solid filtered off under reduced pressure and dried in the vacuum oven to give N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-[(2-methylprop-2-en-1-yl)oxy]-2-nitrobenzamide as an orange solid (8.73 g); NMR Spectrum (DMSOd6) 0.6 (m, 2H), 0.7 (m, 2H), 1.9 (s, 3H), 2.3 (s, 1H), 2.9 (m, 1H), 4.7 (s, 2H), 5.1 (s, 1H), 5.2 (s, 1H), 7.2 (m, 3H), 7.6 (d, 1H), 7.9 (s, 1H), 8.2 (d, 1H), 8.4 (m, 1H), 10.1 (s, 1H); Mass Spectrum: M+H+ 408.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-a40a0623aae64a0fa47804acfd5513be
Source noteuspto-grants-2010_07