HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612528Generated: October 25, 2026
Melatonin → N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide
https://huagongshe.com/reaction/612528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Melatonin | HCID 896 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide | HCID 23283701 | — |
Reaction Steps
To a solution, cooled to 0° C., of melatonin (1 mmol) in trifluoroacetic acid (2 ml) is added dropwise borane (2 eq, 1M solution in THF) . The mixture is stirred for 30 min at 0° C. followed by dropwise addition of water (1.5 ml), and the medium is left stirring for 1 h at room temperature. The mixture is then brought to pH=10 using 2N potassium hydroxide solution and is then extracted with dichloromethane. The crude product is separated on a column of flash silica (25/75/5 acetone/dichloromethane/methanol) and 110 mg of N-[2-(5-methoxyindolin-3-yl)ethyl]acetamide are obtained, which product is then acetylated with acetic anhydride in pyridine to give N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06004991 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-6772556b0a354ecaad31a1198c92fd86 |
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| Source note | uspto-grants-1999_12 |
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