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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383807Generated: October 26, 2026

(1-methyl-1H-imidazol-4-yl)methanamine → N-((1-Methyl-1H-imidazol-4-yl)methyl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamide

https://huagongshe.com/reaction/383807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-methyl-1H-imidazol-4-yl)methanamineHCID 2795114—
ReactantLithium 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 68787401—
ProductN-((1-Methyl-1H-imidazol-4-yl)methyl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamideHCID 59636775—

Reaction Steps

The compound was prepared according to the procedure disclosed in Example 1 starting from lithium 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate (70 mg, 0.18 mmol) and (1-methyl-1H-imidazol-4-yl)methylamine (24 mg, 0.22 mmol). Yield: 42 mg (48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367676B2
Source datasetuspto-grants-2013_02
ORD IDord-0cc56fe4456c491b83de55dab79feb88
Source noteuspto-grants-2013_02