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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420372Generated: October 30, 2026

(Pyridin-4-yl)boronic acid → 4-{2-(2-Ethoxycarbony-ethyl)-3-[6-(3-pyridin-4-yl-5-thiophen-3-yl-phenoxy)-hexyl]-phenoxy}-butyric acid ethyl ester

https://huagongshe.com/reaction/420372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant4-{3-[6-(3-Iodo-5-thiophen-3-yl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy}-butyric acid ethyl esterHCID 57586538—
Product4-{2-(2-Ethoxycarbony-ethyl)-3-[6-(3-pyridin-4-yl-5-thiophen-3-yl-phenoxy)-hexyl]-phenoxy}-butyric acid ethyl esterHCID 5758647062.1%

Reaction Steps

A similar procedure as described in Example 12, step 8 was used, starting from 4-{3-[6-(3-iodo-5-thiophen-3-yl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy}-butyric acid ethyl ester (207 mg, 0.3 mmol) and pyridin-4-ylboronic acid (123 mg, 1.0 mmol) to obtain 4-{2-(2-ethoxycarbony-ethyl)-3-[6-(3-pyridin-4-yl-5-thiophen-3-yl-phenoxy)-hexyl]-phenoxy}-butyric acid ethyl ester (120 mg, 62%) as an yellow oil: ES(+)-HRMS m/e calculated for C38H45NO6S (M+H)+ 644.3041, found 644.3041.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093385B2
Source datasetuspto-grants-2012_01
ORD IDord-a4beace8d8ba4c7a95faeb1e08083cdc
Source noteuspto-grants-2012_01