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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715533Generated: October 27, 2026

3-Amino-4-bromo-6-chloropyridazine → 6-Chloro-4-methylpyridazin-3-amine

https://huagongshe.com/reaction/715533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-4-bromo-6-chloropyridazineHCID 22024419—
ReactantHCID 178477796HCID 178477796—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product6-Chloro-4-methylpyridazin-3-amineHCID 12353664100.6%

Reaction Steps

A 100 mL flask was charged with 4-bromo-6-chloropyridazin-3-amine (1 g, 4.80 mmol), dimethylzinc (9.59 mL, 9.59 mmol), Pd(PPh3)4 (0.277 g, 0.240 mmol) and DMF (10 mL). The reaction mixture was stirred at RT. Then the reaction mixture was quenched with MeOH and concentrated. The crude product was loaded onto a 10 g SCX SPE, and 3 volumes of MeOH followed by 3 volumes of 2N ammonia in MeOH were added. The fractions were combined and concentrated to afford 6-chloro-4-methylpyridazin-3-amine (693 mg, 80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187464B2
Source datasetuspto-grants-2015_11
ORD IDord-7940148f828a48ffb205f7dbaa5c6526
Source noteuspto-grants-2015_11