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HRID 394853作成日:2026年10月24日

Sodium Hydroxide → 5-Hydrazino-2-pyridinesulfonamide hydrochloride

https://huagongshe.com/ja/reaction/394853

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Stannous chloride dihydrateHCID 61436—
反応物5-Aminopyridine-2-sulfonamideHCID 22313850—
反応物Sodium NitriteHCID 23668193—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Hydrochloride methanolHCID 21893726—
生成物5-Hydrazino-2-pyridinesulfonamide hydrochlorideHCID 2231382956%

反応手順

To a suspension of 5-amino-2-pyridinesulfonamide (7.0 g, 0.040 mol, C. Komfeld, J. Amer. Chem. Soc. 1695 (1942)) in conc HCl (60 mL) and H2O (20 mL), sodium nitrite (3.6 g, 0.052 mol) in H2O (50 mL) was added dropwise at 0° C. and the mixture was stirred for 30 min. The mixture changed to yellow brown solution and tin(II) chloride dihydrate (36 g, 0.16 mol) in conc HCl (30 mL) was added dropwise below 5° C. and stirred for 1 hour at 0° C. The mixture was made basic by addition of aqueous NaOH (pH=8). The resultant suspension was added THF (400 mL) and stirred for 10 min. The white precipitate was separated by celite filtration and washed with THF (100 mL×3). The filtrate was separated in two phase and organic phase was separated. Water phase was extracted with THF (150 mL×2), dried (MgSO4), and concentrated in vacuo gave brown oil. The oil was disolved in 10% HCl-MeOH (50 mL) and concentrated in vacuo gave brown amorphous solid. Crystallization from CH2Cl2 gave the titled compound as a brown solid (5.0 g, 56%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06603008B1
出典データセットuspto-grants-2003_08
ORD IDord-3a40d48f132c447e892e1ca757dd14c3
出典メモuspto-grants-2003_08