Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535634Generated: October 26, 2026

1-Phenylpiperidin-4-amine → N-(1-Phenylpiperidin-4-yl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamide

https://huagongshe.com/reaction/535634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenylpiperidin-4-amineHCID 21193347—
ReactantLithium 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 68787401—
ProductN-(1-Phenylpiperidin-4-yl)-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamideHCID 59636723—

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-phenylpiperidin-4-amine (39 mg, 0.22 mmol). Yield: 34 mg (34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-0b66843abb7d45dfa73293c6a74e0b17
Source noteuspto-grants-2014_10