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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533766Generated: October 27, 2026

3-methoxy-4-(2-methoxy-1H-benzimidazol-4-yl)carbonylamino-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide → HCID 178492694, compound

https://huagongshe.com/reaction/1533766

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methoxy-4-(2-methoxy-1H-benzimidazol-4-yl)carbonylamino-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamideHCID 18354872—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178492694HCID 17849269439%

Reaction Steps

A solution of 3-methoxy-4-(2-methoxy-1 H-benzimidazol-4-yl)carbonylamino-N-methyl-N-(4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (139 mg) in 10% hydrogen chloride in methanol (2 ml) was stirred at ambient temperature for 2 hours and 4 N hydrogen chloride in 1,4-dioxane (2 ml) was added to the mixture. After being allowed to stand at ambient temperature overnight, the reaction mixture was concentrated in vacuo and the residue was diluted with a mixture of chloroform and saturated aqueous sodium bicarbonate solution. The organic layer was separated and washed with water and brine. The solution was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (chloroform-methanol=10:1) to give 4-(2-hydroxy-1 H-benzimidazol-4-yl)carbonylamino-3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (53 mg) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207693B1
Source datasetuspto-grants-2001_03
ORD IDord-9af16c8cc94444cf80b2fb1e7be90191
Source noteuspto-grants-2001_03