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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739143Generated: November 3, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-Nitro-2-(3,5-dimethylphenyl)benzoyl methionine methyl ester

https://huagongshe.com/reaction/1739143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
Reactant2-(3,5-Dimethylphenyl)-4-nitrobenzoic acidHCID 23436225—
ReactantN-BOC-4-aminobenzoyl methionine methyl esterHCID 67564255—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product4-Nitro-2-(3,5-dimethylphenyl)benzoyl methionine methyl esterHCID 1866676358.4%

Reaction Steps

4-nitro-2-(3,5-dimethylphenyl)benzoic acid (0.15 g, 0.55 mmol), methionine methyl ester hydrochloride salt (0.11 g, 0.55 mmol), EDCI (0.11 g, 0.55 mmol), HOBT (0.07 g, 0.55 mmol) and Et3N (0.08 ml) in dry CH2Cl2 (2.2 ml) were reacted and worked up according to the procedure for N-BOC-4-aminobenzoyl methionine methyl ester in Example 1. After recrystallization from ethyl acetate and hexanes, 0.13 g (58.4%) of pure product was isolated. mp 122-124° C.; 1H NMR (CDCl3) 1.2-1.84 (1H, m), 1.85-1.97 (1H, m), 2.01 (3H, s), 2.05 (3H, t, J=7.7 Hz), 2.38 (6H, s), 3.70 (3H, s), 4.67-4.74 (1H, m), 6.03 (1H, d, J=7.9 Hz), 7.05 (2H, s), 7.09 (1H, s), 7.84-7.87 (1H, m), 7.84-7.87 (1H, m), 8.23-8.26 (2H, m); 13C NMR (CDCl3), 15.20, 21.26, 29.22, 31.15, 51.79, 52.57, 122.07, 25.11, 126.27, 130.03, 130.53, 137.77, 138.82, 140.29, 141.56, 148.41, 167.14, 171.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965539
Source datasetuspto-grants-1999_10
ORD IDord-bb3d2e8fd31f4079999a359ea9bd69fa
Source noteuspto-grants-1999_10