Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255941Generated: October 31, 2026

N-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamide → 3-(cinnolin-4-ylethynyl)-N-{3-cyclopropyl-4-[(4-methylpiperazin-1-yl)methyl]phenyl}-4-methylbenzamide

https://huagongshe.com/reaction/1255941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamideHCID 46839047—
Reactant4-EthynylcinnolineHCID 57775151—
Product3-(cinnolin-4-ylethynyl)-N-{3-cyclopropyl-4-[(4-methylpiperazin-1-yl)methyl]phenyl}-4-methylbenzamideHCID 57775090—

Reaction Steps

The title compound can be synthesized from 4-ethynylcinnoline and N-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamide in a manner similar to that described for Example 1 (nitro reduction performed in a manner similar to that described for Example 10; 0.25M in MeOH/10% AcOH). 4-ethynylcinnoline is prepared from 4-bromocinnoline and ethynyltrimethylsilane according to the 2 steps procedure described in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461167B2
Source datasetuspto-grants-2013_06
ORD IDord-3573f348fd5349eb9f0dfaea108b2e09
Source noteuspto-grants-2013_06