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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706831Generated: October 31, 2026

N-cyclopropyl-6-ethynylpyridazin-3-amine → 3-(2-(6-(Cyclopropylamino)pyridazin-3-yl)ethynyl)-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/706831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-cyclopropyl-6-ethynylpyridazin-3-amineHCID 86709556—
Reactant3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3(trifluoromethyl)phenyl)benzamideHCID 86709562—
Product3-(2-(6-(Cyclopropylamino)pyridazin-3-yl)ethynyl)-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamideHCID 72949914—

Reaction Steps

The title compound was synthesized from N-cyclopropyl-6-ethynylpyridazin-3-amine and 3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl) benzamide (as prepared above) in a manner similar to that described for in Example 1. The product was obtained as a pale yellow solid. Mp:125-126° C.; 1H NMR (300 MHz, CDCl3) δ: 9.94 (1 H, s), 8.34 (1 H, s), 8.20-8.23 (1 H, d, J=8.7 Hz), 8.02 (1 H, s), 7.86-7.89 (1 H, d, J=8.1 Hz), 7.53 (1 H, s), 7.39-7.42 (1 H, d, J=9.0 Hz), 7.30-7.32 (2 H, m), 7.02-7.05 (1 H, d, J=9.2 Hz), 6.80 (1 H, s), 6.02 (1 H, s), 2.58 (1 H, m), 2.48 (3 H, s), 2.29 (3 H, s), 0.87 (2 H, m), 0.64 (2 H, brs). HRMS (ESI-TOF+): m/z [M+2H]+2 calcd for C28H25F3N6O: 259.1015. found: 259.1023.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174996B2
Source datasetuspto-grants-2015_11
ORD IDord-94a1723ccb6b4c458bacb2b9281f9e9a
Source noteuspto-grants-2015_11