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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535859Generated: October 30, 2026

3-Ethynylimidazo[1,2-b]pyridazine → 4-Chloro-3-(2-(imidazo[1,2-b]pyridazin-3-yl)ethynyl)-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/535859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethynylimidazo[1,2-b]pyridazineHCID 46838760—
Reactant4-chloro-3-iodo-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamideHCID 86709564—
Product4-Chloro-3-(2-(imidazo[1,2-b]pyridazin-3-yl)ethynyl)-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamideHCID 72950418—

Reaction Steps

The title compound was synthesized from 3-ethynylimidazo[1,2-b]pyridazine and 4-chloro-3-iodo-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide in a manner similar to that described for in Example 1. The title compound was obtained as a light yellow solid. Mp: 153-154° C.; 1H NMR (300 MHz, CDCl3) δ: 9.35 (1H, s), 8.48-8.49 (1H, d, J=3.6 Hz), 8.25 (1H, s), 8.15 (2H, brs), 7.89-7.92 (4H, m), 7.57-7.60 (1H, d, J=8.4 Hz), 7.37 (1H, s), 7.12-7.16 (1H, dd, J=4.2 and 9.3 Hz), 2.27 (3H, s). HRMS (ESI-TOF+): m/z [M+2H]+2 calcd for C26H18ClF3N6O: 261.0586. found: 261.0584.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859553B2
Source datasetuspto-grants-2014_10
ORD IDord-0ad6820650ee47ca93ae004108c80ad4
Source noteuspto-grants-2014_10