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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739131Generated: November 3, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-BOC-4-amino-3-methylbenzoyl methionine methyl ester

https://huagongshe.com/reaction/1739131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
Reactant4-{[(Tert-butoxy)carbonyl]amino}-3-methylbenzoic acidHCID 15432029—
ReactantN-BOC-4-aminobenzoyl methionine methyl esterHCID 67564255—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-BOC-4-amino-3-methylbenzoyl methionine methyl esterHCID 6756638185.7%

Reaction Steps

N-BOC-4-amino-3-methylbenzoic acid (2.00 g, 7.96 mmol) was reacted with methionine methyl ester hydrochloride (1.75 g, 8.76 mmol), EDCI (1.68 g, 8.76 mmol), HOBT (1.18 g, 8.76 mmol) and Et3N (1.4 ml) in dry CH2Cl2 (31.8 ml) according to the procedure described for N-BOC-4-aminobenzoyl methionine methyl ester in Example 1. The crude material was recrystallized from ethyl acetate and hexanes to yield 2.61 g (85.7%) of pure product. mp 163-165° C.; 1H NMR (CDCl3) 1.54 (9H, s), 2.06-2.18 (4H, m), 2.23-2.34 (4H, m), 2.59 (2H, t, J=6.8 Hz), 3.80 (3H, s), 4.92 (1H, m), 6.45 (1H, s), 6.88 (1H, d, J=7.5 Hz), 7.63 (1H, d, J=8.6 Hz), 7.66 (1H, s), 8.05 (1H, d, J=8.6); 13C NMR (CDCl3) 15.47, 17.61, 28.22, 30.03, 31.55, 51.93, 52.57, 81.04, 118.73, 125.62, 127.66, 129.54, 139.89, 152.34, 166.58, 172.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965539
Source datasetuspto-grants-1999_10
ORD IDord-485f92186b3d44d1b458569598929428
Source noteuspto-grants-1999_10