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HRID 216662作成日:2026年10月27日

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

https://huagongshe.com/reaction/216662

反応式

関与物質

役割名称HCID仕込み量
反応物BromoacetoneHCID 11715—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 178455413HCID 178455413—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒SulfolaneHCID 31347—
生成物6-(Tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-imidazo[1,2-a]pyrazineHCID 13172975340%

反応条件

温度50 °C

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193236B2
出典データセットuspto-grants-2012_06
ORD IDord-00dcd9c4425745448596a956681b4ee5
出典メモuspto-grants-2012_06