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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239822Generated: October 27, 2026

Bromine → 4-Bromo-6-chloro-5-methylpyridazin-3-amine

https://huagongshe.com/reaction/2239822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Chloro-5-methylpyridazin-3-amineHCID 12353663—
Reactant6-Chloro-4-methylpyridazin-3-amineHCID 12353664—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-6-chloro-5-methylpyridazin-3-amineHCID 59624331—

Reaction Steps

The mixture of 6-chloro-5-methylpyridazin-3-amine and 3-chloro-5-methylpyridazin-6-amine (1.45 g, 10 mmol) from 1a and NaHCO3 (2.1 g, 25 mmol) were suspended in MeOH (20 mL) and treated with Br2 (0.57 mL, 11 mmol). The mixture was stirred at room temperature for 4 h, then filtered. The filtrate was condensed in vacuo. The resulting residue was resuspended in EtOAc (100 mL) and washed sequentially with sat. aqueous NaHCO3 solution (2×20 mL) and aqueous NaCl solution (1×20 mL). The solution was dried over MgSO4. The solvent was removed in vacuo to give crude 4-bromo-6-chloro-5-methylpyridazin-3-amine (1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-e3c58a78953b4cfb8d08e35ebd2f641b
Source noteuspto-grants-2010_05