HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36112Erstellt: 23. Oktober 2026
Methanol → 6-[(1-Oxopentyl)amino]-2-butyl-5-methylimidazo[4,5-b]pyridine
https://huagongshe.com/de/reaction/36112
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Pentanoic Acid | HCID 7991 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | 4-Methyl-3,5-dinitropyridin-2-amine | HCID 5086399 | — |
| Katalysator | Nickel | HCID 935 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 6-[(1-Oxopentyl)amino]-2-butyl-5-methylimidazo[4,5-b]pyridine | HCID 19939780 | — |
Reaktionsschritte
A mixture of 2-amino-3,5-dinitro-4-methylpyridine (5.2 g, 26 mmol), THF (100 mL), methanol (1300 mL) and Raney-nickel (3 mL of a 1:1 suspension in H2O) was stirred under H2 (1 atm.) for 5 h. The mixture was quickly filtered into a flask containing 3 ml of conc. HCl and the solvent was removed in vacuo at r.t. To the resulting crude 2,3,5-triamino-6-methylpyridine HCl complex was added valeric acid (8.68 mL, 80 mmol) and polyphosphoric acid (100 mL) and this mixture was heated to 80° C. for 7 h. The warmed mixture was poured into stirred ice-H2O (500 mL) and this mixture was cooled and neutralized (to pH 3) by the addition of conc. NH4OH. Extraction with CH2Cl2 (5×50 mL), drying (Na2SO4), concentration and purification (SiO2, 5% MeOH/EtOAc) gave the title compound as a solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05412097 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-6de85dba48e842268fe764ab41bd33f6 |
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| Quellennotiz | uspto-grants-1995_05 |
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