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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992483Generated: October 25, 2026

2-Chloropyridine-4-boronic acid → 1-{4-[1-(2-Chloro-pyridin-4-yl)-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carbonyl]-piperazin-1-yl}-2-methyl-propan-1-one

https://huagongshe.com/reaction/1992483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloropyridine-4-boronic acidHCID 5151595—
Reactant1-{4-[5-(4-Isopropyl-piperazine-1-carbonyl)-1H-indole-2-carbonyl]-piperazin-1-yl}-2-methyl-propan-1-oneHCID 68533986—
Product1-{4-[1-(2-Chloro-pyridin-4-yl)-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carbonyl]-piperazin-1-yl}-2-methyl-propan-1-oneHCID 8662193343%

Reaction Steps

The title compound was synthesized in analogy to example 5, after stirring for 6.5 days at 35° C., from 1-{4-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carbonyl]-piperazin-1-yl}-2-methyl-propan-1-one (example 31) and 2-chloropyridine-4-boronic acid to afford the desired product as light-brown foam (43%). MS (ISP): 565.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648979B2
Source datasetuspto-grants-2010_01
ORD IDord-d26c0a39015441c1920ce7e24f65268c
Source noteuspto-grants-2010_01