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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706806Generated: October 30, 2026

2-(3-Iodo-4-methylphenyl)-6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazole → N-Isopropyl-6-(2-(2-methyl-5-(6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)phenyl)ethynyl)pyridazin-3-amine

https://huagongshe.com/reaction/706806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Iodo-4-methylphenyl)-6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazoleHCID 86709555—
ReactantN-isopropyl-6-ethynylpyridazin-3-amineHCID 86709557—
ProductN-Isopropyl-6-(2-(2-methyl-5-(6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)phenyl)ethynyl)pyridazin-3-amineHCID 72949555—

Reaction Steps

The title compound was synthesized from N-isopropyl-6-ethynylpyridazin-3-amine and 2-(3-iodo-4-methylphenyl)-6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]-imidazole (as prepared in Example 1) in a manner similar to that described for in Example 1. The intermediate compound N-isopropyl-6-ethynylpyridazin-3-amine was made as for Example 1 (Step 1 to 3) with the spectra below: 1H NMR (300 MHz, CDCl3) δ: 7.26-7.29 (1 H, d, J=9.0 Hz), 6.54-6.57 (1 H, d, J=9.0 Hz), 5.00 (1 H, s), 3.97-4.04 (1 H, m), 3.25 (1 H, s), 1.29 (3 H, s), 1.27 (3 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174996B2
Source datasetuspto-grants-2015_11
ORD IDord-fd5e345aacb543e0bac6f4e01277f326
Source noteuspto-grants-2015_11