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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493990Generated: October 27, 2026

Pyridine → 5-[2-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-pyridine-2-carbonitrile

https://huagongshe.com/reaction/493990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Cyanopyridine-5-boronic acid pinacol esterHCID 16414188—
Reactant(1,1-Dioxo-thiomorpholin-4-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanoneHCID 16739577—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product5-[2-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-pyridine-2-carbonitrileHCID 1673960830.6%

Reaction Steps

To a mixture of (1,1-dioxo-thiomorpholin-4-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (Example 2, 150 mg, 1.0 eq.), anhydrous copper(II) acetate (131 mg, 2 eq.), pyridine (120 microL, 4 eq.) in dichloromethane (3.5 mL), 2-cyanopyridine-5-boronic acid pinacol ester (247 mg, 3 eq.) was added. The reaction mixture was stirred for 4 days and then concentrated in vacuo. The residue was then purified on silica eluting with dichloromethane/methanol 98:2 v:v. One fraction was isolated and dried in vacuo, to yield 57 mg (23%) of the desired product as light yellow oil. MS (m/e): 522.5 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538101B2
Source datasetuspto-grants-2009_05
ORD IDord-7bbeb58ec3ce4bbaa3f7fdac473dd3ca
Source noteuspto-grants-2009_05