Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755312Generated: November 4, 2026

Bromine → Methyl 4-(6-amino-5-bromopyridazin-3-yl)benzoate

https://huagongshe.com/reaction/1755312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4-(6-aminopyridazin-3-yl)benzoateHCID 86682704—
SolventMethanolHCID 887—
ProductMethyl 4-(6-amino-5-bromopyridazin-3-yl)benzoateHCID 8668270543.6%

Reaction Steps

In a 250 mL round bottom flask was placed methyl 4-(6-aminopyridazin-3-yl)benzoate (2.8 g, 12.2 mmol), NaHCO3 (2.05 g, 22.4 mmol) and methanol (100 mL) and to this suspension was added Br2 (1.95 g, 12.2 mmol) drop wise over about 30 minutes at room temperature. The mixture was stirred for 16 h, then filtered and concentrated in vacuo. The residue was purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=2:1) to give methyl 4-(6-amino-5-bromopyridazin-3-yl)benzoate (1.64 g, 43.6%) as a light orange solid. LC-MS: [M+H]+, 309.9, tR=1.397 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169259B2
Source datasetuspto-grants-2015_10
ORD IDord-7fcaa08492df47a086575e9da87316fc
Source noteuspto-grants-2015_10