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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739128Generated: November 1, 2026

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

https://huagongshe.com/reaction/1739128

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-{[(Tert-butoxy)carbonyl]amino}benzoic acidHCID 2755931—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-BOC-4-aminobenzoyl methionine methyl esterHCID 6756425571.3%

Reaction Steps

Into a dried, nitrogen filled flask was placed N-BOC-4-aminobenzoic acid (8.77 g, 36.97 mmol) in dry CH2Cl2 (148 ml) along with methionine methyl ester hydrochloride (8.12 g, 40.66 mmol). This solution was cooled in an ice bath and triethylamine (6.7 ml), EDCI (7.80 g, 40.66 mmol) and hydroxybenzotriazole (HOBT, 5.50 g, 40.66 mmol) were added. The mixture was stirred overnight, diluted with more CH2Cl2 and was extracted 3 times each with 1M HCl, 1M NaHCO3 and water. The CH2Cl2 was dried over MgSO4 and the solvent was removed in vacuo. The solid was recrystallized from ethyl acetate/ hexanes to yield 9.72 g (71.3%) of pure product. mp 184-185° C.; 1H NMR (CDCl3) 1.53 (9H, s), 2.06-2.18 (4H, m), 2.23-2.33 (1H, m), 2.59 (2H, t, J=7.6 Hz), 3.80 (3H, s), 4.92 (1H, m), 7.45 (2H, d, J=8.7 Hz), 7.77 (2H, d, J=8.7 Hz); 13C NMR (CDCl3) 15.59, 28.34, 30.15, 31.64, 52.10, 52.73, 81.20, 117.73, 127.8, 128.33, 141.88, 152.33, 166.50, 172.75; anal. calc. for C18H26N2O5S, C: 56.53, H: 6.85, N: 7.29; found, C: 56.47, H: 6.86, N: 7.29; m/ z (EI) 382 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965539
Source datasetuspto-grants-1999_10
ORD IDord-f7b68109e4f04f1a83b51e75fc329519
Source noteuspto-grants-1999_10