HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18226Generated: October 25, 2026
N,1-dimethyl-1H-indole-3-carboxamide → 1-Methyl-3-(methylaminomethyl)indole
https://huagongshe.com/reaction/18226
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,1-dimethyl-1H-indole-3-carboxamide | HCID 5152277 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Methyl-3-(methylaminomethyl)indole | HCID 10986778 | 67% |
Reaction Steps
A solution of LiAlH4 in THF (1.0 M, 5.20 mL, 5.2 mmole) was slowly added via syringe to a solution of N,1-dimethyl-1H-indole-3-carboxamide (0.50 g, 2.6 mmole) in anhydrous THF (15 mL). Gas was evolved during the addition of the first 2 mL of LiAlH4 solution. When the addition was complete, the resulting light yellow solution was heated at gentle reflux. After 23 hr, the reaction was cooled in ice and quenched by the sequential dropwise addition of H2O (0.5 mL), 1.0 N NaOH (0.5 mL), and H2O (0.5 mL). The mixture was stirred for 15 min, then was filtered through Celite®, and the filter pad was washed thoroughly with THF. The filtrate was concentrated and the residue was flash chromatographed on silica gel (10% MeOH/CHCl3 containing 0.5% conc. NH4OH) to afford the title compound (0.30 g, 67%) as a light yellow oil: MS (ES) m/e 175 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741339B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-e26fc45da9cb41cf8a7f24875da07a33 |
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| Source note | uspto-grants-2010_06 |
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