HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-dimethyl-6-nitropyridin-3-amine → N5,N5-Dimethylpyridine-2,5-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-dimethyl-6-nitropyridin-3-amine | HCID 21897368 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N5,N5-Dimethylpyridine-2,5-diamine | HCID 5743468 | — |
Reaction Steps
The N,N-dimethyl-6-nitropyridine-3-amine obtained above is taken up in 25 ml of ethanol. After addition of 4.8 g of stannous chloride, the reaction mixture is heated at reflux for 30 minutes and then concentrated to dryness. The residue is chromatographed on a column of silica (40-63 μm), elution being carried out with a mixture of dichloromethane and ammoniacal methanol (90/10). The fractions comprising the expected product are combined and concentrated to give 750 mg of 5-dimethylaminopyridine-2-amine in the form of a pasty yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08404848B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-6bcaa530a1064a8396fe4f976d3c3632 |
| Source note | uspto-grants-2013_03 |