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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535639Generated: October 26, 2026

1-(3-Chloropyridin-2-YL)piperidin-4-amine → N-(1-(3-Chloropyridin-2-yl)piperidin-4-yl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamide

https://huagongshe.com/reaction/535639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chloropyridin-2-YL)piperidin-4-amineHCID 12760108—
ReactantLithium 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 68787401—
ProductN-(1-(3-Chloropyridin-2-yl)piperidin-4-yl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamideHCID 59636728—

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 (80 mg, 0.21 mmol) and 1-(3-chloropyridin-2-yl)piperidin-4-amine (57 mg, 0.27 mmol). Yield: 50 mg (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-1cc2030b882046a49b6c8feab0eda577
Source noteuspto-grants-2014_10