Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774211Generated: November 4, 2026

Water → HCID 86696711, compound

https://huagongshe.com/reaction/1774211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86696649HCID 86696649—
ReactantHCID 86696712HCID 86696712—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86696711HCID 8669671126%

Reaction Conditions

Temperature70 °C

Reaction Steps

KOt-Bu (224 mg, 2 mmol) and n-Bu4NI (37 mg, 0.1 mmol) were added to a mixture of tert-butyl 2-((methylsulfonyloxy)methyl)-1H-indole-1-carboxylate (350 mg, 1.07 mmol) and 4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one (272 mg, 1 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 2-(((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 2-((2-oxo-4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-1(2H)-yl)methyl)-1H-indole-1-carboxylate (130 mg, 26% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09259470B2
Source datasetuspto-grants-2016_02
ORD IDord-d0a14f5a12484e9d8af10dabc69638c9
Source noteuspto-grants-2016_02