HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutylamine → 5-Methyl-7-isobutylamino-1H-pyrazolo[4,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | 7-Chloro-5-methyl-1H-pyrazolo[4,3-b]pyridine | HCID 11679871 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Methyl-7-isobutylamino-1H-pyrazolo[4,3-b]pyridine | HCID 20254852 | 40.8% |
Reaction Steps
A mixture of 7-chloro-5-methyl-1H-pyrazolo[4,3-b]pyridine (1.0 g, 0.006 mole) and isobutylamine (58 g) in water (100 ml) and ethanol (50 ml) was heated under reflux for 10 days. The reaction mixture was cooled and evaporated to dryness. The oily residue was basified to pH8-9 with 10% sodium carbonate solution. The residue was extracted with ethyl acetate (3×100 ml), dried (Na2SO4) and evaporated to dryness to give a yellow oil. This was purified by column chromatography on alumina, and eluted with chloroform/methanol to give the desired compound as a white solid (500 mg). m.p. 162°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04559348 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-1e35a82176b84261aec90207eee6f937 |
| Source note | uspto-grants-1985_12 |