HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220178Generated: October 26, 2026
4-Bromoaniline → 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (4-bromo-phenyl)-amide
https://huagongshe.com/reaction/220178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid | HCID 59238266 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (4-bromo-phenyl)-amide | HCID 59238294 | — |
Reaction Steps
To a solution of 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (1.9 g, 6.5 mmol), Et3N (3.6 mL, 26 mmol), and Pybrop (6 g, 13 mmol) in CH2Cl2 (30 mL) was added 4-bromo-phenylamine (1.45 g, 8.45 mmol). This mixture was stirred overnight at room temperature and then evaporated. The mixture was redissolved in EtOAc (40 mL) and washed with 2N HCl (20 mL×3), brine, 5% NaHCO3 (20 mL×3), brine, dried with Na2SO4, filtered and evaporated. The residue was purified by column chromatography on silica gel using hexane/EtOAc to give a white solid (1.63 g, 56% for two steps). MS: calc'd 444 (MH+), exp 444 (MH+). 1H NMR (400 MHz, CDCl3-d) 9.65 (broad s, 1H), 8.72 (d, 1H, J=2.0 Hz), 8.06 (d, 1H, J=8.4 Hz), 7.53-7.41 (m, 4H), 4.18-4.08 (m, 1H), 3.66-3.54 (m, 2H), 2.45-2.35 (m, 1H), 2.21-2.11 (m, 1H), 1.98-1.87 (m, 1H), 1.83-1.72 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08202866B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-37abab0d833d4ed6b72a3cd9ac56a8c5 |
|---|
| Source note | uspto-grants-2012_06 |
|---|