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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594650Generated: October 27, 2026

Methyl N-(3-nitrobenzoyl)-3-amino-3-(3,4-dimethoxyphenyl)propionate → Methyl N-(3-aminobenzoyl)-3-amino-3-(3,4-dimethoxyphenyl)propionate

https://huagongshe.com/reaction/1594650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl N-(3-nitrobenzoyl)-3-amino-3-(3,4-dimethoxyphenyl)propionateHCID 15547129—
ReactantDichloromethane ethylacetateHCID 21226138—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductMethyl N-(3-aminobenzoyl)-3-amino-3-(3,4-dimethoxyphenyl)propionateHCID 1554713093%

Reaction Steps

To a solution of methyl N-(3-nitrobenzoyl)-3-amino-3-(3,4-dimethoxyphenyl)propionate (1.25 grams, 3.22 mmol) in a mixture of 150 milliliters of ethyl acetate and 75 milliliters of methanol (mixture gently warmed to dissolve all solid and then allowed to cool to room temperature) was added 0.25 grams of 10% Pd/C. The mixture was then treated with 60 psi of H2 for 2.5 hours on a Parr Type Shaker. Reaction progress was monitored by TLC (1/9 ethyl acetate/methylene chloride, UV) and was complete after 2.5 hours. The reaction mixture was filtered through celite to remove catalyst. The filtrate was concentrated in vacuo to afford a white solid which was dried in vacuo (60 ° C., <1 mm) to afford 1.07 grams (93%) of the desired product: 1H NMR (dmso-d6, 250 MHz) δ 8.60 (d, J=8.5 Hz, 1 H, NH), 7.15-6.8 (m, 6 H, Ar), 6.67 (m, 1 H, Ar), 5.40 (m, 1 H, CHCO), 5.24 (m 2 H, ArNH2), 3.75 (s, 3 H, OCH3), 3.72 (s, 3 H, OCH3), 3.56 (s, 3 H, CO2CH3), 2.95 (dd, J=8.9, 15.4 Hz, 1 H), 2.81 (dd, J=6.3, 15.4 Hz, 1 H); 13C NMR (dmso-d6) δ 170.9, 166.4, 148.6, 148.6, 147.8, 135.6, 135.1, 128.6, 118.5, 116.4, 114.4, 112.8, 111.6, 110.6, 55.5, 55.5, 51.4, 49.6, 40.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284780B1
Source datasetuspto-grants-2001_09
ORD IDord-c31d891c724846fcba72947b0febdf6a
Source noteuspto-grants-2001_09