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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19862Generated: October 28, 2026

(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanone → 5-[2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-pyridine-2-carbonitrile

https://huagongshe.com/reaction/19862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
Reactant2-Cyanopyridine-5-boronic acid pinacol esterHCID 16414188—
Product5-[2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-pyridine-2-carbonitrileHCID 16739526—

Reaction Steps

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 2-cyanopyridine-5-boronic acid pinacol ester. The title compound was obtained in 51% yield as yellow foam. MS (m/e): 508.4 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745479B2
Source datasetuspto-grants-2010_06
ORD IDord-821e20648b564e72adb4ec731e111843
Source noteuspto-grants-2010_06