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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219260Generated: October 27, 2026

3,6-Dichloropyridazine → 3-Chloro-6-(3-methylisothiazol-5-yl)pyridazine

https://huagongshe.com/reaction/219260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-DichloropyridazineHCID 67331—
Reactant5-Bromo-3-methylisothiazoleHCID 600959—
ReactantHCID 178418918HCID 178418918—
CatalystZincchlorideHCID 3007855—
CatalystDitert-butyl(cyclopenta-2,4-dien-1-yl)phosphane;iron(2+);(2,3,4,5-tetraphenylcyclopenta-1,4-dien-1-yl)benzeneHCID 129828017—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-6-(3-methylisothiazol-5-yl)pyridazineHCID 57691326—

Reaction Steps

To a solution of 5-bromo-3-methylisothiazole (2.42 g, 14 mmol) in 20 mL of THF at −45° C. was added isopropylmagnesium chloride (19 ml, 19 mmol) in THF (1 M). After 20 minutes, zinc(II) chloride (41 ml, 20 mmol) in THF (0.5 M) was added and the solution was warmed up to rt. 3,6-dichloropyridazine (2.4 g, 16 mmol), 3,6-dichloropyridazine (2.4 g, 16 mmol) and Q-Phos (2.5 g) were added and the reaction was heated to 50° C. for 16 hours. The reaction was then cooled to 23° C. and quenched with 60 mL of satd. NH4Cl aq. solution. The mixture was mixed with celite and 100 mL of EtOAc. The insoluble material was removed by filtration. The filtrate was diluted with 40 mL of EtOAc and 30 mL of water. The organic phase was separated and washed with 60 mL of brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (10% to 80% hex/EtOAc) to afford red solid as desired product. MS (ESI pos. ion) m/z: 212 (MH+). Calc'd exact mass for C8H6ClN3S: 211.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198448B2
Source datasetuspto-grants-2012_06
ORD IDord-1f8f1c962d3741b1a3853b7adc1d7c79
Source noteuspto-grants-2012_06