Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945751Generated: October 29, 2026

1,4-Dioxane → HCID 59605558, compound

https://huagongshe.com/reaction/1945751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant4-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-c]pyridineHCID 58356446—
Reactant2-(1-((9-Methyl-6-morpholino-2-(tributylstannyl)-9H-purin-8-yl)methyl)piperidin-4-yl)propan-2-olHCID 59605536—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
CatalystHCID 178418397HCID 178418397—
ProductHCID 59605558HCID 5960555886%

Reaction Conditions

Temperature150 °C

Reaction Steps

A 20 mL microwave vial was charged with a suspension of 2-[1-(9-methyl-6-morpholin-4-yl-2-(tributylstannanyl)-9H-purin-8-ylmethyl)piperidin-4-yl]propan-2-ol (0.5 g, 0.75 mmol), 1-benzenesulfonyl-4-bromo-1H-pyrrolo[2,3-c]pyridine (0.29 g, 0.83 mmol), CuTC (0.029 g, 0.015 mmol) and Pd(PPh3)4 (0.087 g, 0.075 mmol) in dioxane (8 mL). The reaction mixture was heated in a microwave for 30 min at 150° C. The cooled reaction mixture was loaded onto an SCX-2 cartridge. The cartridge was washed with 3 volumes of MeOH, then the product was recovered eluting with 2N ammonia in MeOH. The solution was concentrated and the residue loaded onto a 40 g SiO2 column and purified by flash chromatography (Si—PCC; 40 g SiO2 column, 0% to 6% MeOH in DCM) to give 2-{1-[2-(1-Benzenesulfonyl-2-methyl-1H-pyrrolo[2,3-c]pyridin-4-yl)-9-methyl-6-morpholin-4-yl-9H-purin-8-ylmethyl]piperidin-4-yl}propan-2-ol as white foam (0.414 g, 86%). LCMS (Method A): RT=3.24 min, [M+H]+ 645.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-c3d02ac0cc39465fbbd3a40608ad0ef2
Source noteuspto-grants-2013_03