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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356079Generated: October 30, 2026

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

https://huagongshe.com/reaction/356079

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—
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 CH2C12 (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 (9 H,s), 2.06-2.18 (4 H, m), 2.23-2.34 (4 H, m), 2.59 (2 H, t, J=6.8 Hz), 3.80 (3 H, s), 4.92 (1 H, m), 6.45 (1 H, s), 6.88 (1 H, d, J=7.5 Hz), 7.63 (1 H, d, J=8.6 Hz), 7.66 (1 H, s), 8.05 (1 H, 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 numberUS05834434
Source datasetuspto-grants-1998_11
ORD IDord-bac7711aacd44a7a9d96bb8a92ecf709
Source noteuspto-grants-1998_11