HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565031Generated: October 31, 2026
Phenylacetaldehyde → Ethyl 1-methyl-7-(2-phenylethylamino)-2-indolecarboxylate
https://huagongshe.com/reaction/565031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 7-amino-1-methyl-2-indolecarboxylate | HCID 21194578 | — |
| Reactant | Sodium cyanogen borohydride | HCID 131722252 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 1-methyl-7-(2-phenylethylamino)-2-indolecarboxylate | HCID 21194741 | 30.5% |
Reaction Steps
A mixture of 0.10 g (0.46 mmol) of ethyl 7-amino-1-methyl-2-indolecarboxylate, 0.12 g (0.50 mmol) of phenylacetaldehyde as 50% isopropanol solution, 0.043 g (0.69 mmol) of sodium cyanogen borohydride and 0.1 ml of acetic acid in 5 ml of acetonitrile was stirred at room temperature for 15 minutes. Thereafter 0.2 ml of acetic acid was added to the reaction mixture. The resulting mixture was allowed to stand at room temperature for 15 hours. After 1N sodium hydroxide solution was added to the reaction mixture, the mixture was extracted three times with diethyl ether. The combined extracts were then washed with 1N potassium hydroxide solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to give 0.045 g (30.5%) of ethyl 1-methyl-7-(2-phenylethylamino)-2-indolecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169107A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-ecdde33ada3045b6a0b223c2d05349c9 |
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| Source note | uspto-grants-2001_01 |
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