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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388475Generated: October 31, 2026

1,1'-Carbonyldiimidazole → (S)-2-(2-amino-4-methoxy-benzoylamino)-hexanoic acid methyl ester

https://huagongshe.com/reaction/388475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Amino-4-methoxybenzoic acidHCID 351010—
Reactantmethyl (2S)-2-aminohexanoate hydrochlorideHCID 14039065—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product(S)-2-(2-amino-4-methoxy-benzoylamino)-hexanoic acid methyl esterHCID 6872925559%

Reaction Steps

To a solution of 2-amino-4-methoxy-benzoic acid (1.0 g, 5.98 mmol) and 1,1′-carbonyldiimidazole (980 mg, 6.04 mmol) in pyridine (5 mL) is added 1,8-diazabicyclo[5.4.0]undec-7-ene (0.9 mL, 6.02 mmol). The mixture is stirred at room temperature for 2 hours follows by the addition of (S)-2-amino-hexanoic acid methyl ester hydrochloride (1.1 g, 6.06 mmol). The reaction mixture is stirred at room temperature for 16 hours and diluted with EtOAc (100 mL), the solution is washed with H2O (50 mL×3). The organic layer is dried over sodium sulfate, and is concentrated. The resulting residue is purified by flash chromatography with 60% EtOAc in hexanes as the eluent to afford (S)-2-(2-amino-4-methoxy-benzoylamino)-hexanoic acid methyl ester (1.03 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377949B2
Source datasetuspto-grants-2013_02
ORD IDord-8bfc118369f54071991b23aa6fcb154a
Source noteuspto-grants-2013_02