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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522805Generated: October 30, 2026

2-(Tributylstannyl)pyridine → 2,6-Bis-((R)-3-methyl-morpholin-4-yl)-8-pyridin-2-yl-9-(tetrahydro-pyran-2-yl)-9H-purine

https://huagongshe.com/reaction/522805

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)pyridineHCID 607784—
Reactant8-Bromo-2,6-bis-((R)-3-methyl-morpholin-4-yl)-9-(tetrahydro-pyran-2-yl)-9H-purineHCID 89525639—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product2,6-Bis-((R)-3-methyl-morpholin-4-yl)-8-pyridin-2-yl-9-(tetrahydro-pyran-2-yl)-9H-purineHCID 8952574288%

Reaction Conditions

Temperature120 °C

Reaction Steps

8-Bromo-2,6-bis-((R)-3-methyl-morpholin-4-yl)-9-(tetrahydro-pyran-2-yl)-9H-purine (40 mg, 83 μmol) was dissolved in 2 mL of toluene under argon in a microwave vial, and 2-(tributylstannyl)-pyridine (36 mg, 83 μmol) and Pd(PPh3)4 (4.8 mg, 4.2 μmol) were added. The microwave vial was capped, and the reaction mixture was stirred for 3 hours at 120° C. The vial was cooled to room temperature and opened. The mixture was diluted with EtOAc (20 mL) and brine. The organic layer was separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (12 g SiO2, heptane/TBME in a gradient from 4/1 to 2/3) to give the product as a solid (35 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334271B2
Source datasetuspto-grants-2016_05
ORD IDord-89f2a9df4ae94a1ca443b9b2bce2c2a4
Source noteuspto-grants-2016_05