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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498789Generated: October 25, 2026

Tributylvinyltin → 3-(3,5-dimethyl-1H-1,2,4-triazol-1-yl)-5-vinylpyridazine

https://huagongshe.com/reaction/1498789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant5-chloro-3-(3,5-dimethyl-1H-1,2,4-triazol-1-yl)pyridazineHCID 86732048—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-(3,5-dimethyl-1H-1,2,4-triazol-1-yl)-5-vinylpyridazineHCID 86732049—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 5-chloro-3-(3,5-dimethyl-1H-1,2,4-triazol-1-yl)pyridazine (23-2, 730 mg, 3.48 mmol, 1.0 eq.) in toluene (24 mL) were added tetrakis(triphenylphosphine)palladium(0) (200 mg, 0.17 mmol, 0.05 eq.) and tributyl(vinyl)tin (1.30 mL, 4.52 mmol, 1.3 eq.). The mixture was heated at 120° C. for 3 hours. The solvent was removed under reduced pressure and the resulting residue was purified by silica gel column chromatography (30% ethyl acetate in hexanes) to afford 3-(3,5-dimethyl-1H-1,2,4-triazol-1-yl)-5-vinylpyridazine (23-3) as a white solid. 1H NMR (300 MHz, CDCl3) δ 9.15 (d, 1H, J=1.8 Hz), 8.02 (d, 1H, J=1.8 Hz), 6.73 (dd, 1H, J=17.7, 10.8 Hz), 6.23 (d, 1H, J=17.7 Hz), 5.78 (d, 1H, J=10.8 Hz), 2.95 (s, 3H), 2.44 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200001B2
Source datasetuspto-grants-2015_12
ORD IDord-f01f87dd0e4d4c619b3cbfda8f6bba81
Source noteuspto-grants-2015_12