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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216662Generated: October 25, 2026

Bromoacetone → 6-(Tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-imidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/216662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetoneHCID 11715—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178455413HCID 178455413—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSulfolaneHCID 31347—
Product6-(Tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-imidazo[1,2-a]pyrazineHCID 13172975340%

Reaction Conditions

Temperature50 °C

Reaction Steps

Bromoacetone (4.3 g, 31.4 mmol, 2.9 equiv) is added to a solution of 5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrazin-2-ylamine (4.0 g, 10.7 mmol) in 1,2-dimethoxyethane (20 ml) and sulfolane (20 ml). The reaction mixture is stirred overnight at 50° C. Then a 10% aqueous solution of NaHCO3 (30 ml) is added, and the mixture is heated to reflux for 1 hour. After cooling, the mixture is extracted three times with EtOAc. The combined organic layers are washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (hexane/EtOAc 3:1) affords the title compound (1.7 g, 40%). 1H NMR (400 MHz, d6-DMSO): δ=8.78 (d, J=0.9 Hz, 1H), 8.43 (d, J=1.4 Hz, 1H), 7.92 (s, 1H), 7.63-7.61 (m, 4H); 7.41-7.35 (m, 6H), 4.72 (s, 2H), 2.34 (s, 3H), 1.00 (s, 9H). MS (ES+): 402 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193236B2
Source datasetuspto-grants-2012_06
ORD IDord-00dcd9c4425745448596a956681b4ee5
Source noteuspto-grants-2012_06