HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83624Generated: October 30, 2026
O-Methyltyramine → HCID 66571280, compound
https://huagongshe.com/reaction/83624
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methyltyramine | HCID 4657 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid | HCID 57385796 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66571280 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846684B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a6913922e1504e9a9ccfc47016193f58 |
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| Source note | uspto-grants-2014_09 |
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