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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535854Generated: October 27, 2026

3-Iodo-4-methyl-N-[3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]benzamide → 3-(2-(6-(Isopropylamino)pyridazin-3-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/535854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Iodo-4-methyl-N-[3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]benzamideHCID 17752158—
ReactantN-isopropyl-6-ethynylpyridazin-3-amineHCID 86709557—
Product3-(2-(6-(Isopropylamino)pyridazin-3-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamideHCID 72950252—

Reaction Steps

The title compound was synthesized from N-isopropyl-6-ethynylpyridazin-3-amine and 3-iodo-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide in a manner similar to that described for in Example 1. The product was obtained as a pale yellow solid. Mp: 192-194° C.; 1H NMR (300 MHz, DMSO-d6) δ: 10.73 (1H, s), 8.33 (1H, s), 8.17-8.22 (2H, m), 7.94-7.96 (1H, d, J=7.2 Hz), 7.76 (1H, s), 7.54-7.57 (1H, d, J=7.8 Hz), 7.45-7.48 (1H, d, J=8.4 Hz), 7.15-7.18 (1H, d, J=7.5 Hz), 6.79-6.82 (1H, d, J=9.0 Hz), 4.14-4.20 (1H, m), 2.56 (3H, s), 2.19 (3H, brs), 1.20-1.22 (6H, d, J=6.3 Hz). HRMS (ESI-TOF+): m/z [M+H]+ calcd for C28H26F3N6O: 519.2115. found: 519.2121.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859553B2
Source datasetuspto-grants-2014_10
ORD IDord-a044b665085c45faaf44c805328f2663
Source noteuspto-grants-2014_10