Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971109Generated: November 1, 2026

3-Acetylphenylboronic acid → HCID 22391970, compound

https://huagongshe.com/reaction/971109

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acetylphenylboronic acidHCID 2734310—
Reactant1-(3-bromophenyl)-N-isopropyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamideHCID 12991318—
Reactant2-(5-Bromopyridin-2-yl)propan-2-olHCID 15486392—
ProductHCID 22391970HCID 22391970—

Reaction Steps

Following the procedure of Step 5 of Example 1, but substituting 3-aminophenylboronic acid for 3-acetyl phenylboronic acid and 5-bromo-2-(1-hydroxy-1-methylethyl)pyridine from Step 1 of Example 30 for N-isopropyl-1-(3-bromophenyl)-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide, the 5-(3-Aminophenyl)-2-(1-hydroxy-1-methylethyl)pyridine compound was obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312334B2
Source datasetuspto-grants-2007_12
ORD IDord-fc2df323a68d43cb87806d3e54c1d133
Source noteuspto-grants-2007_12