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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365855Generated: October 31, 2026

Water → HCID 86696709, compound

https://huagongshe.com/reaction/2365855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86696649HCID 86696649—
ReactantHCID 86696710HCID 86696710—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86696709HCID 8669670923.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

KOt-Bu (180 mg, 1.6 mmol) and n-Bu4NI (37 mg, 0.1 mmol) were added to a mixture of tert-butyl 6-((methylsulfonyloxy)methyl)-1H-indole-1-carboxylate (0.8 mmol) and 4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one (164 mg, 0.6 mmol) in anhydrous THF (15 mL). The resulting mixture was stirred at 70° C. under microwave irradiation for 2 hours. LC-MS showed the tert-butyl 6-(((methylsulfonyl)oxy)methyl)-1H-indole-1-carboxylate had disappeared. The reaction mixture was treated with water (20 mL) and diluted with dichloromethane. After removal of the insolubles by filtration, the filtrate was extracted with dichloromethane. The combined organic phase was dried with Na2SO4 and concentrated. The residue was purified with Combiflash (A: H2O including 0.5% NH3HCO3, B: CH3CN) to afford tert-butyl 6-((2-oxo-4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-1(2H)-yl)methyl)-1H-indole-1-carboxylate (70 mg, 23% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697715B2
Source datasetuspto-grants-2014_04
ORD IDord-5d08c785db214f3d95e8210853c6b0b9
Source noteuspto-grants-2014_04