HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335186Generated: October 29, 2026
Ethyl Acetate → Methyl 4-(2-amino-5-bromopyridin-3-ylthio)benzoate
https://huagongshe.com/reaction/335186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Methyl 4-(2-aminopyridin-3-ylthio)benzoate | HCID 66994709 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 4-(2-amino-5-bromopyridin-3-ylthio)benzoate | HCID 66994425 | 68% |
Reaction Steps
Placed methyl 4-(2-aminopyridin-3-ylthio)benzoate (5.50 g, 21.1 mmol) in acetic acid (25 mL) and cooled to 0° C. Slowly added bromine (1.35 mL, 26.4 mmol) and stirred for an hour. Poured reaction mixture onto saturated sodium bisulfite and ice. Extracted with dichloromethane three times, washed with 2N NaOH, water, brine, dried, and concentrated. Subjected to MPLC (Biotage) eluting with 3:2 hexane:ethyl acetate to afford the title compound (4.87 g, 68.0% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883828B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3a83b713d15c4039a6749731b311fde7 |
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| Source note | uspto-grants-2014_11 |
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