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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806112Generated: October 30, 2026

Ethyl Acetate → Methyl 4-(2-amino-5-bromopyridin-3-ylthio)benzoate

https://huagongshe.com/reaction/1806112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBromineHCID 24408—
ReactantSodium BisulfiteHCID 23665763—
ReactantMethyl 4-(2-aminopyridin-3-ylthio)benzoateHCID 66994709—
SolventAcetic AcidHCID 176—
ProductMethyl 4-(2-amino-5-bromopyridin-3-ylthio)benzoateHCID 6699442568%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354540B2
Source datasetuspto-grants-2013_01
ORD IDord-2750437c1bb844c18207dc1e45056ae6
Source noteuspto-grants-2013_01