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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535637Generated: October 25, 2026

1-(4-Aminopiperidin-1-yl)ethan-1-one → N-(1-Acetylpiperidin-4-yl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamide

https://huagongshe.com/reaction/535637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminopiperidin-1-yl)ethan-1-oneHCID 4962477—
ReactantLithium 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 68787401—
ProductN-(1-Acetylpiperidin-4-yl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamideHCID 59636752—

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 (60 mg, 0.16 mmol) and 1-(4-amino-piperidin-1-yl)-ethanone (27 mg, 0.19 mmol). Yield: 39 mg (47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-2132658f28a043cc8d6924b4b61bb789
Source noteuspto-grants-2014_10