HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butanamine, 1-methoxy- → HCID 22249609, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butanamine, 1-methoxy- | HCID 93837 | — |
| Reactant | HCID 22249907 | HCID 22249907 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 22249609 | HCID 22249609 | — |
Reaction Steps
A solution of 4-chloro-3-(2-chloroethyl)-8-mesityl-2-methyl[1,5]naphthyridine (200 mg, 0.557 mmol) in 2-amino-1-methoxybutane (2.0 mL) was stirred at 200° C. for four hours in a sealed tube. After overnight, the residue was purified by silica gel column chromatography (30-50% ethylacetate/hexane) Activated manganese dioxide (290 mg, 3.24 mmol) was added to a solution of the resulting product (130 mg, 0.33 mmol) in toluene (20 mL) and the mixture was heated under reflux for one day. After filtering through Celite, the mixture was evaporated. The residue was purified by silica gel column chromatography-(10% ethyl acetate/hexane), to give the title compound (108 mg) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06927221B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-ad01b8120168446b9aa940a089e7885a |
| Source note | uspto-grants-2005_08 |