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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706826Generated: October 31, 2026

4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide → 4-Chloro-3-(2-(6-(cyclopropylamino)pyridazin-3-yl)ethynyl)-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/706826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamideHCID 71562635—
ReactantN-cyclopropyl-6-ethynylpyridazin-3-amineHCID 86709556—
Product4-Chloro-3-(2-(6-(cyclopropylamino)pyridazin-3-yl)ethynyl)-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamideHCID 72949911—

Reaction Steps

The title compound was synthesized from N-cyclopropyl-6-ethynylpyridazin-3-amine and 4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl) benzamide in a manner similar to that described for in Example 1. The intermediate compound 4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide was made as for Example 12 (Step 1 to 4) with the spectra below: 1H NMR (300 MHz, DMSO-d6) δ: 10.66 (1 H, s), 8.53 (1 H, s), 8.19 (1 H, s), 8.02-8.05 (1 H, d, J=6.0 Hz), 7.98-8.01 (1 H, d, J=6.0 Hz), 7.77 (1 H, s), 7.70-7.73 (1 H, d, J=6.0 Hz), 3.62 (2 H, s), 3.33 (2 H, m), 2.82 (2 H, m), 2.54 (4 H, m), 2.50 (3 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174996B2
Source datasetuspto-grants-2015_11
ORD IDord-76ed2edfc8fa4d91b7e3dc02fb2aef72
Source noteuspto-grants-2015_11