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HRID 425894作成日:2026年10月25日

N-bromobutanimide → 3-(Benzyloxy)-5-bromopyridin-2-amine

https://huagongshe.com/reaction/425894

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物2-Amino-3-benzyloxypyridineHCID 90334—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物3-(Benzyloxy)-5-bromopyridin-2-amineHCID 2062655453%

反応手順

To a stirred solution of 2-amino-3-benzyloxypyridine (42.0 g, 0.21 mol) in CH3CN (600 mL) at 0° C. was added N-bromosuccinimide (37.1 g, 0.21 mol) over 30 minutes. The mixture was stirred for 0.5 hr, after which the reaction was then diluted with EtOAc (900 mL) and partitioned with H2O (900 mL). The organic layer was, washed with brine and dried (Na2SO4), filtered and concentrated to dryness under vacuum to yield 3-benzyloxy-5-bromo-pyridin-2-ylamine (31.0 g, 0.11 mol, 53%). 1H NMR (CDCl3, 300 MHz) δ 4.63-4.78 (brs, 2H), 5.04 (s, 2H), 7.07 (d, 1H, J, 1.8 Hz), 7.33-7.42 (m, 5H), 7.73 (d, 1H, J, 1.8 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08106197B2
出典データセットuspto-grants-2012_01
ORD IDord-c82cf1b949b640d692dc8323f8b26d6f
出典メモuspto-grants-2012_01