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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385738Generated: November 1, 2026

2-Chloropyridine-5-boronic acid → 5-(6-Chloropyridin-3-yl)-2-nitrothiophene-3-carboxamide

https://huagongshe.com/reaction/385738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloropyridine-5-boronic acidHCID 3845034—
Reactant5-[6-(1-Hydroxy-1-methylethyl)pyridin-3-yl]-2-nitrothiophene-3-carboxamideHCID 59525801—
Product5-(6-Chloropyridin-3-yl)-2-nitrothiophene-3-carboxamideHCID 59525648—

Reaction Steps

The title compound was prepared from 5-bromo-2-nitrothiophene-3-carboxamide (Intermediate 10 Step 4) (2.0 g, 7.97 mmol) and 2-chloro-5-pyridine boronic acid (1.25 g, 7.97 mmol) according to the general procedure described in Intermediate 10 Step 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-e5a2af8a8c984420bf339732100f7745
Source noteuspto-grants-2013_02