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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387128Generated: October 31, 2026

2-(4-Aminophenyl)benzo[b]thiophene-3-yl 4-[2-(1-pyrrolidinyl)ethoxy]phenyl ketone → 2-(4-Aminophenyl)-3-[4-(2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene

https://huagongshe.com/reaction/1387128

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminophenyl)benzo[b]thiophene-3-yl 4-[2-(1-pyrrolidinyl)ethoxy]phenyl ketoneHCID 22462724—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Aminophenyl)-3-[4-(2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiopheneHCID 2246279285%

Reaction Steps

By essentially following the conditions described in Example 179, Part A, the free base of the title compound was prepared as an oil from 2-(4-aminophenyl)benzo[b]thiophene-3-yl 4-[2-(1-pyrrolidinyl)ethoxy]phenyl ketone (Part C) in 85% yield following MPLC (SiO2; 30% then 40% THF with 5% TEA in hexanes). The product was converted to the oxalate salt according to the conditions described in Example 1, Part G.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-4c0297fc9b4c435680c3230c047d7020
Source noteuspto-grants-2001_07