HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Methyl 6-(benzyl(2-ethoxy-2-oxoethyl)amino)-5-nitronicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl 6-chloro-5-nitronicotinate | HCID 346961 | — |
| Reactant | Methyl 2-(benzylamino)acetate | HCID 422659 | — |
| Product | Methyl 6-(benzyl(2-ethoxy-2-oxoethyl)amino)-5-nitronicotinate | HCID 59416801 | 90% |
Reaction Steps
Methyl 6-chloro-5-nitronicotinate (2.0 g, 9.23 mmol) was added to methyl 2-(benzylamino)acetate (6.0 g, 31.05 mmol) neat while stirring at room temperature. The viscous yellow reaction was heated to 90° C. for one h and then allowed to cool back to room temperature. The reaction was diluted with dichloromethane (20 mL) and purified via column chromatography (220 g SiO2, 20-30% gradient, ethyl acetate in hexanes) to yield the title compound (3.10 g, 90% yield) as a yellow oil. [M+H] calc'd for C18H19N3O6, 374. found, 374.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124606B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-19f53c1788474e708613d68133aa9666 |
| Source note | uspto-grants-2012_02 |