HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Ethyl 3-(2-amino-5-bromopyridin-4-yloxy)-4-chlorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 3-(2-aminopyridin-4-yloxy)-4-chlorobenzoate | HCID 66617829 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 3-(2-amino-5-bromopyridin-4-yloxy)-4-chlorobenzoate | HCID 66617810 | 61.4% |
Reaction Steps
A flask was charged with ethyl 3-(2-aminopyridin-4-yloxy)-4-chlorobenzoate (5.50 g, 18.8 mmol) and acetic acid (50 mL), and bromine (0.943 ml, 18.4 mmol) was added. The reaction was stirred at ambient temperature for 30 minutes and then concentrated. The residue was purified by silica gel column chromatography, eluting with 20%-35% ethyl acetate in hexanes to give the desired product (4.20 g, 58.9% yield) as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022222B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-acb1015a38cd4fb2a8527bc7d186e04d |
| Source note | uspto-grants-2011_09 |