HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848708Generated: October 31, 2026
4-Bromobenzylamine → N-(4-Bromobenzyl)-5-((5-methylpyridin-2-yl)methoxy)-2-nitroaniline
https://huagongshe.com/reaction/1848708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzylamine | HCID 77571 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-((3-Fluoro-4-nitrophenoxy)methyl)-5-methylpyridine | HCID 90411084 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(4-Bromobenzyl)-5-((5-methylpyridin-2-yl)methoxy)-2-nitroaniline | HCID 90410173 | 86.6% |
Reaction Steps
A mixture of 2-((3-fluoro-4-nitrophenoxy)methyl)-5-methylpyridine (2.0 g, 7.6 mmol), 4-bromobenzyl amine (1.6 g, 8.4 mmol), DIPEA (2.63 mL, 15.3 mmol) and acetonitrile (25.4 mL) were sealed in a reaction vessel and heated to 60° Celsius for 24 h. The mixture was cooled to RT, transferred to a round bottomed flask and concentrated to dryness. The crude mixture was heated to 70° Celsius in a minimum amount of i-PrOH until homogeneous and cooled to RT. The resulting mixture was filtered to collect the yellow solids which were dried to afford the title compound (2.82 g, 86%). MS (ESI): mass calcd. for C20H18BrN3O3, 427.053; m/z found, 428.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08952177B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-b886f18200164e86a4cf797a9c60e2e2 |
|---|
| Source note | uspto-grants-2015_02 |
|---|