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HRID 216662생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/216662

반응식

참여 물질

역할이름HCID투입량
반응물BromoacetoneHCID 11715—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178455413HCID 178455413—
용매1,2-DimethoxyethaneHCID 8071—
용매SulfolaneHCID 31347—
생성물6-(Tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-imidazo[1,2-a]pyrazineHCID 13172975340%

반응 조건

온도50 °C

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193236B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-00dcd9c4425745448596a956681b4ee5
출처 메모uspto-grants-2012_06