HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2308089Erstellt: 25. Oktober 2026
HCID 20746075, Verbindung → HCID 20746058, Verbindung
https://huagongshe.com/reaction/2308089
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | HCID 20746075 | HCID 20746075 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 5-Amino-2-methylindole-1-carboxylic acid methylamide | HCID 20746057 | 24% |
| Produkt | HCID 20746058 | HCID 20746058 | 26% |
Reaktionsschritte
To a stirred solution of 2-methyl-5-nitro-indole-1-carboxylic acid methylamide (0.65 g, 2.78 mmol) in 20 mL EtOAc and 4 mL EtOH was added Pd on C (0.3 g, 10% w/w). The mixture was stirred under H2 balloon at room temperature for one hour and filtered through a pad of silica gel. The filtrate was concentrated in vacuo. The residue was purified by flash column chromatography eluting with 1-3% MeOH in CH2Cl2 to give 140 mg 5-amino-2-methyl-indole-1-carboxylic acid methylamide (24% yield) together with 150 mg 5-amino-2-methyl-2,3-dihydro-indole-1-carboxylic acid methylamide (26% yield). 1H NMR (300 MHz, CD3OD) δ 7.56 (d, 1H, J=6.2 Hz), 6.65 (s, 1H), 6.58 (d, 1H, J=6.1 Hz), 4.41 (m, 1H), 3.23-3.39 (m, 1H), 2.85 (s, 3H), 2.54 (d, 1H, J=15.5 Hz), 1.20 (d, 3H, J=6 Hz).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06833456B2 |
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| Quelldatensatz | uspto-grants-2004_12 |
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| ORD ID | ord-65353e0805584a0f92cb630574acc702 |
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| Quellennotiz | uspto-grants-2004_12 |
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