HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Chloro-N-(4-methoxybenzyl)-3-nitropyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 2,4-Dichloro-3-nitropyridine | HCID 10535773 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloro-N-(4-methoxybenzyl)-3-nitropyridin-4-amine | HCID 53429445 | 51% |
Reaction Steps
To a solution of 2,4-dichloro-3-nitropyridine (12.0 g, 62.2 mmol) in DMF (78 mL) was added NEt3 (10.4 mL, 74.6 mmol) and p-methoxybenzylamine (8.12 ml, 62.18 mmol) at 0° C. After stirring for 10 h at rt, DMF was removed at reduced pressure. The residue was triturated with EtOAc, filtered, washed with EtOAc and hexane, and dried to afford 2-chloro-N-(4-methoxybenzyl)-3-nitropyridin-4-amine (9.29 g, 51%). Additional product (8.0 g, 44%) was obtained by column chromatography (SiO2, eluent) from the filtrates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017780B1 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-c67a54d9294a4ba18731161673050a33 |
| Source note | uspto-grants-2011_09 |