Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753171Generated: November 2, 2026

Potassium Carbonate → HCID 67367823, compound

https://huagongshe.com/reaction/1753171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
ReactantHCID 67370128HCID 67370128—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 67367823HCID 67367823105.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 10a-(4-hydroxyphenyl)-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (50 mg, 0.19 mmol) and potassium carbonate (77 mg, 0.56 mmol) in DMF (1 mL) was added (2-bromoethoxy)-tert-butyldimethylsilane (120 μL, 0.56 mmol). The mixture was heated at 100° C. The outcome of the reaction was monitored by LCMS. After completion (45 minutes) the mixture was diluted with a saturated aqueous solution of NH4Cl (6 mL) and extracted with ethyl acetate (3×2.5 mL). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo to yield a pale yellow solid that was purified by flash chromatography (Biotage SP4, 12 g silica cartridge, gradient 0-10% MeOH in CH2Cl2) to give 10a-[4-(2-{[tert-butyl(dimethyl)silyl]oxy]ethoxy)phenyl}-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (86 mg, quantitative yield). ESI-MI m/z [M+H]+ 428.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163029B2
Source datasetuspto-grants-2015_10
ORD IDord-30138ccb9c42499c947af1a23d86080a
Source noteuspto-grants-2015_10