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HRID 1056002作成日:2026年10月27日

Aniline → 8-bromo-3-methyl-N-phenylquinoxalin-2-amine

https://huagongshe.com/reaction/1056002

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物5-Bromo-3-chloro-2-methylquinoxalineHCID 89428887—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物8-bromo-3-methyl-N-phenylquinoxalin-2-amineHCID 8978208271%

反応手順

LHMDS (1.0M in THF; 14.37 ml, 14.37 mmol) was added to a solution of 5-bromo-3-chloro-2-methylquinoxaline (126e, 0.74 g, 2.87 mmol) and aniline (1.309 ml, 14.37 mmol, Alfa Aesar, Ward Hill, Mass.) in dioxane (28.7 ml) at RT, and the resulting mixture was stirred at RT for 30 min. The mixture was diluted with EtOAc (200 ml), added to a separatory funnel, and washed with saturated aq. NH4Cl (2×150 ml) before the organic layer was separated, dried over Na2SO4, and concentrated. Purification by silica gel (100% hexanes to 20% EtOAc/hexanes) provided 8-bromo-3-methyl-N-phenylquinoxalin-2-amine (183a, 71% yield) as a brown oil. MS (ESI, pos. ion) m/z: 314.2/316.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09394297B2
出典データセットuspto-grants-2016_07
ORD IDord-2e342e456a10458b950e04da86d5375f
出典メモuspto-grants-2016_07