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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992487Generated: October 25, 2026

2-Chloropyridine-5-boronic acid → [1-(6-Chloro-pyridin-3-yl)-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-(4-cyclopropanesulfonyl-piperazin-1-yl)-methanone

https://huagongshe.com/reaction/1992487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloropyridine-5-boronic acidHCID 3845034—
Reactant(4-Cyclopropanesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanoneHCID 68535679—
Product[1-(6-Chloro-pyridin-3-yl)-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-(4-cyclopropanesulfonyl-piperazin-1-yl)-methanoneHCID 8662193644%

Reaction Steps

The title compound was synthesized in analogy to example 5, from (4-cyclopropanesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone (example 33) and 2-chloropyridine-5-boronic acid to afford the desired product as light brown foam (44%). MS (ISP): 599.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648979B2
Source datasetuspto-grants-2010_01
ORD IDord-fa8cc329eec54398965db67e0f7cb1fb
Source noteuspto-grants-2010_01