HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348512Generated: October 30, 2026
HCID 17810719, compound → HCID 17810717, compound
https://huagongshe.com/reaction/348512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 17810719 | HCID 17810719 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 17810717 | HCID 17810717 | 90% |
Reaction Steps
829 mg (6 mmol) of 2-nitroaniline and 1242 mg (7.8 mmol) of 1-methylindole carboxyaldehyde were dissolved in 20 ml of tetrahydrofuran followed by the sequential addition of 200 μl of acetic acid and 5087 mg (24 mmol) of NaBH(OAc)3 and stirring overnight at room temperature. After adding saturated aqueous sodium bicarbonate solution, extracting with ethyl acetate and drying with anhydrous magnesium sulfate, the solvent was distilled off and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5) to obtain 264 mg of ((1-methylindole-3-yl)methyl)(2-nitrophenyl)amine (yield: 18%). 264 mg (0.939 mmol) of ((1-methylindole-3-yl)methyl)(2-nitrophenyl)amine were then dissolved in 10 ml of ethanol followed by the addition of 50 mg (0.047 mmol) of 10% Pd—C and stirring for 6 hours at room temperature in a hydrogen atmosphere. After completion of the reaction, the Pd—C was filtered out and the solvent was distilled off under reduced pressure to obtain 212 mg of ((1-methylindole-3-yl)methyl)(2-aminophenyl)amine (yield: 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176320B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-d761bcac4ab24090a0cc22654f31a6f8 |
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| Source note | uspto-grants-2007_02 |
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