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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706813Generated: October 29, 2026

N-isopropyl-6-ethynylpyridazin-3-amine → 6-(2-(2-Chloro-5-(6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)phenyl)ethynyl)-N-isopropylpyridazin-3-amine

https://huagongshe.com/reaction/706813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-isopropyl-6-ethynylpyridazin-3-amineHCID 86709557—
Reactant2-(4-chloro-3-iodophenyl)-6-((4-methylpiperazin-1-yl)methyl)-1H-benzoimidazoleHCID 86709558—
Product6-(2-(2-Chloro-5-(6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)phenyl)ethynyl)-N-isopropylpyridazin-3-amineHCID 72949731—

Reaction Steps

The title compound was synthesized from N-isopropyl-6-ethynylpyridazin-3-amine and 2-(4-chloro-3-iodophenyl)-6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazole in a manner similar to that described for in Example 1. The title compound was obtained as a khaki solid. Mp:127-128° C.; 1H NMR (300 MHz, CDCl3) δ: 8.11-8.13 (1 H, d, J=6.0 Hz), 7.82 (1 H, s), 7.64 (2 H, m), 7.53 (1 H, s), 7.35-7.38 (1 H, d, J=9.0 Hz), 7.29-7.32 (1 H, d, J=9.0 Hz), 6.66-6.69 (1 H, d, J=9.0 Hz), 5.22 (1 H, s), 4.12-4.14 (1 H, m), 3.62 (2 H, s), 2.51 (8 H, brs), 2.31 (3 H, s), 1.25-1.31 (6 H, m). HRMS (ESI-TOF+): m/z [M+H]+ calcd for C28H31ClN7: 500.2324. found: 500.2313.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174996B2
Source datasetuspto-grants-2015_11
ORD IDord-8dce29dd1d0b4ea194c8f4aea7f989dd
Source noteuspto-grants-2015_11