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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528487Generated: October 29, 2026

Sodium Carbonate → HCID 86711762, compound

https://huagongshe.com/reaction/528487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Indolylboronic acidHCID 2734361—
Reactant2-Chloro-7,7-dimethyl-4-morpholin-4-yl-6,7-dihydro-[1,4]dioxino[2,3-d]pyrimidineHCID 86711747—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
ProductHCID 86711762HCID 8671176217%

Reaction Conditions

Temperature120 °C

Reaction Steps

A microwave vial was charged with 2-chloro-7,7-dimethyl-4-morpholin-4-yl-6,7-dihydro-[1,4]dioxino[2,3-d]pyrimidine from Example 104 (50 mg, 0.18 mmol), 5-indolylboronic acid (42 mg, 0.26 mmol), Pd(PPh3)2Cl2 (12 mg, 0.02 mmol) and sodium carbonate (0.5 mL, 0.5 mmol, 1M aqueous solution) in acetonitrile (1.5 mL) then evacuated and back filled with nitrogen before being heated to 120° C. for 30 minutes using microwave irradiation. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge which was washed with methanol and the product eluted with 2M ammonia in methanol. The basic fractions were combined and concentrated in vacuo. The resulting residue was purified by reverse phase HPLC (Phenomenex Gemini 5 μm C18, 0.1% HCO2H in water on a gradient of acetonitrile 5-98%) affording 115 as a white solid (11 mg, 17%). LCMS: RT=4.37 min, [M+H]+=367. 1H NMR (400 MHz, CDCl3): δ 8.67 (1H, s), 8.28-8.20 (2H, m), 7.39 (1H, d, J=8.6 Hz), 7.23-7.19 (1H, m), 6.61 (1H, broad s), 3.91 (2H, s), 3.90-3.82 (8H, m), 1.48 (6H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346817B2
Source datasetuspto-grants-2016_05
ORD IDord-96d4f84ef92646d2819eb167ac116665
Source noteuspto-grants-2016_05