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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739137Generated: November 1, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (4-Nitro-2-phenylbenzoyl)methionine methyl ester

https://huagongshe.com/reaction/1739137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Nitro-2-phenylbenzoic acidHCID 10657841—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
ReactantN-BOC-4-aminobenzoyl methionine methyl esterHCID 67564255—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product(4-Nitro-2-phenylbenzoyl)methionine methyl esterHCID 1866676485.8%

Reaction Steps

4-nitro-2-phenylbenzoic acid (0.30 g, 1.23 mmol), methionine methyl ester hydrochloride salt (0.27 g, 1.35 mmol), EDCI (0.26 g, 1.35 mmol), HOBT (0.18 g, 1.35 mmol) and Et3N (0.19 ml) in dry CH2Cl2 (4.9 ml) were reacted according to the above procedure and worked up as described for N-BOC-4-aminobenzoyl methionine methyl ester in Example 1. After recrystallization from ethyl acetate and hexanes, 0.41 g (85.5%) of pure product was isolated. mp 98-101° C.; 1H NMR (CDCl3) 1.62-1.73 (1H, m), 1.79-1.88 (1H, m), 1.91 (3H, s), 1.99 (2H, t, J=7.2 Hz), 3.59 (3H, s), 4.53 (1H, m), 6.45 (1H, d, J=7.8 Hz), 7.33-7.40 (5H, m), 7.67 (1H, d, J=8.3 Hz), 8.07-8.12 (2H, m); 13C NMR (CDCl3) 14.92, 29.11, 30.67, 51.51, 52.29, 121.86, 124.74, 128.27, 128.60, 128.69, 129.52, 137.50, 140.56, 141.02, 148.09, 167.23, 171.23; m/z (FAB), 389 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965539
Source datasetuspto-grants-1999_10
ORD IDord-9fcb715aca084b78aa28ea44c79ec279
Source noteuspto-grants-1999_10