HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → 2-[(Cyclopropylmethyl)aminocarbonyl]-4-(4-nitrophenoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chloro-2-[(cyclopropylmethyl)aminocarbonyl]pyridine | HCID 34829121 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[(Cyclopropylmethyl)aminocarbonyl]-4-(4-nitrophenoxy)pyridine | HCID 22936897 | — |
Reaction Steps
4-Chloro-2-[(cyclopropylmethyl)aminocarbonyl]pyridine (1.5 g), p-nitrophenol (2.0 g), Hunig's base (3.1 ml) and 1-methyl-2-pyrrolidinone (6.2 ml) were stirred together at 160° C. for 3 hours. Water was added, extraction was performed with ethyl acetate, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography (hexane:ethyl acetate=4:1, followed by 2:1) using NH type silica gel to obtain 0.35 g of the target substance as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612092B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-6c521d8f1c744ce780cd35425a43d828 |
| Source note | uspto-grants-2009_11 |