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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83624Generated: October 30, 2026

O-Methyltyramine → HCID 66571280, compound

https://huagongshe.com/reaction/83624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethyltyramineHCID 4657—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acidHCID 57385796—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66571280HCID 66571280—

Reaction Steps

1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (100 mg, 0.252 mmol), EDCI (72.5 mg, 0.378 mmol), and 1-hydroxybenzotriazole (51.1 mg, 0.378 mmol) were dissolved in DCM (Volume: 3.0 ml). The reaction was stirred at room temperature for 10 minutes before Hunig'sBase (0.066 ml, 0.378 mmol) and 2-(4-methoxyphenyl)ethanamine (0.055 ml, 0.378 mmol) were added. The reaction was allowed to stir overnight at room temperature. The reaction was diluted with water and ethyl acetate. The organic phase was washed with 1N HCl, saturated sodium bicarbonate, and brine. The organic phase was dried over magnesium sulfate, filtered, and concentrated. The crude material was triturated with ethyl acetate to obtain product as a white solid. (Yield: 84 mg, white solid) 1H-NMR (400 MHz, DMSO-d6) 7.80, 7.59, 7.51, 7.34-7.27, 7.23-7.14, 7.12-7.02, 6.84-6.78, 6.68, 5.45, 4.48-3.82, 3.67, 3.18, 2.89, 2.60, 2.34-2.26, 1.59, 1.31

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846684B2
Source datasetuspto-grants-2014_09
ORD IDord-a6913922e1504e9a9ccfc47016193f58
Source noteuspto-grants-2014_09