HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 70975423, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | HCID 86673552 | HCID 86673552 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 70975423 | HCID 70975423 | 73.1% |
Reaction Steps
1.85 g (R)-1-(2-chloro-6-methyl-3-nitropyridin-4-yl)piperidine-3-carbamic acid tert-butyl ester (5 mmol) was dissolved in 10 mL N-methylpyrrolidone, to which 1.4 mL triethylamine (10 mmol) was added, and 1.25 g 2,4-dimethoxybenzylamine (7.5 mmoL) was added. The reaction was continued for 24 h at 80° C. The reaction solution was exacted three times with ethyl acetate. The ethyl acetate phase was combined, washed three times with water, dried, and evaporated to dryness. The resultant crude product was purified through a column chromatography (ethyl acetate:petroleum ether=1:8) to afford 1.83 g titled product with a yield of 73.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680089B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-bc52f337dcd645ceb8bbda0238fab689 |
| Source note | uspto-grants-2014_03 |