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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19887Generated: October 25, 2026

2-Chloropyridine-4-boronic acid → [6-Bromo-1-(2-chloro-pyridin-4-yl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanone

https://huagongshe.com/reaction/19887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloropyridine-4-boronic acidHCID 5151595—
Reactant[6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanoneHCID 67017918—
Product[6-Bromo-1-(2-chloro-pyridin-4-yl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanoneHCID 16739659—

Reaction Steps

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from [6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanone (example 41, step 6) and 2-chloropyridine-4-boronic acid. The title compound was obtained in 12% yield as light yellow oil. MS (m/e): 561.4 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745479B2
Source datasetuspto-grants-2010_06
ORD IDord-ba4b441220114e47a0cb07980cfa53d3
Source noteuspto-grants-2010_06