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HRID 501221作成日:2026年10月26日

Stannous chloride dihydrate → 1-(4-Hydrazinobenzyl)-4-methylpiperazine

https://huagongshe.com/reaction/501221

反応式

関与物質

役割名称HCID仕込み量
反応物Stannous chloride dihydrateHCID 61436—
反応物4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
生成物1-(4-Hydrazinobenzyl)-4-methylpiperazineHCID 6846522299.1%

反応手順

To a stirred solution of 4-[(4-methylpiperazin-1-yl)methyl]aniline (3.2 g, 15.57 mmol) in acetic acid: concentrated HCl (32:32 mL) at 10° C. was added NaNO2 (1.30 g, 18.78 mmol) in water (16 mL) and stirred for 10 min. Freshly prepared SnCl2.2H2O (11.75 g, 51.97 mmol) in concentrated HCl (32 mL) was added at 10° C. The temperature of the reaction mixture was allowed to rise to room temperature and maintained there for 4 hr. After filtering the reaction mixture, the precipitate was washed with water and the solid obtained was dried under reduced pressure to obtain 1-(4-hydrazinobenzyl)-4-methylpiperazine (3.4 g). 1H NMR (CD3OD, 200 MHz) δ: 7.66 (2H, d, J=8.4 Hz), 7.13 (2H, d, J=8.4 Hz), 4.46 (2H, s), 3.72 (8H, bm), 3.11 (3H, s);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772245B2
出典データセットuspto-grants-2010_08
ORD IDord-09f2e740fd884df3b87df1985fce89cf
出典メモuspto-grants-2010_08