HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylcyclohexylamine → N-Cyclohexyl-N-methyl-1H-imidazo[4,5-b]pyridin-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | 5-Chloro-3H-imidazo[4,5-b]pyridine | HCID 5409027 | — |
| Reactant | 7-Chloro-1H-imidazo[4,5-b]pyridine | HCID 12782383 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-Cyclohexyl-N-methyl-1H-imidazo[4,5-b]pyridin-7-amine | HCID 67278157 | — |
Reaction Steps
To a 1:1 mixture (100 mg) of 7-chloro-1H-imidazo[4,5-b]pyridine and 5-chloro-1H-imidazo[4,5-b]pyridine was added N-methylcyclohexanamine (500 ul), and irradiated microwave at 200° C. for 2 hours. The reaction mixture was diluted with chloroform, washed with brine, dried over MgSO4 and evaporated. The residue was purified by flash column chromatography over NH-silica gel with a chloroform/EtOAc (100:1-100:5) as eluant to give N-cyclohexyl-N-methyl-1H-imidazo[4,5-b]pyridin-7-amine (54.8 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163767B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-c0195a0ecfcd49f1ba67e657e682979b |
| Source note | uspto-grants-2012_04 |