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HRID 18215作成日:2026年10月26日

2-Amino-5-bromo-3-nitropyridine → 5-Bromopyridine-2,3-diamine

https://huagongshe.com/reaction/18215

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-5-bromo-3-nitropyridineHCID 138878—
溶媒EthanolHCID 702—
生成物5-Bromopyridine-2,3-diamineHCID 69115698%

反応手順

To a suspension of 2-amino-5-bromo-3-nitropyridine (2.0 g, 9.17 mmole) in absolute EtOH (50 mL) was added SnCl2 hydrate (9.3 g, 41.3 mmole), then the mixture was heated to reflux. After 3 hr the mixture was cooled to RT and concentrated. The residue was taken up in 2.0 M NaOH and extracted with EtOAc (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated to give the title compound (1.69 g, 98%) which was sufficiently pure for use in the next step: MS (ES) m/e 188/190 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741339B2
出典データセットuspto-grants-2010_06
ORD IDord-a6d97c126179416eac70759d445f8bf5
出典メモuspto-grants-2010_06