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HRID 885943作成日:2026年10月27日

Benzylamine → N-benzyl-6-methylpyridazin-3-amine

https://huagongshe.com/reaction/885943

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylamineHCID 7504—
反応物3-Chloro-6-methylpyridazineHCID 227254—
反応物Sodium t-butoxideHCID 23676156—
触媒Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
溶媒TolueneHCID 1140—
生成物N-benzyl-6-methylpyridazin-3-amineHCID 6131350991.3%

反応条件

温度140 °C

反応手順

To a stirred solution of 3-chloro-6-methylpyridazine (215 mg, 1.66 mmol) and benzylamine (267 mg, 2.5 mmol) in toluene (20 mL) was added sodium tert-butoxide (480 mg, 5.0 mmol) and [1,1′-bis(di-tert-butylphosphino)ferrocene]palladium(II) dichloride (20 mg). The reaction mixture was stirred at 140° C. under microwave irradiation for 2 h, then cooled to room temperature and concentrated in vacuo. The residue was purified by column chromatography (SiO2, 0-100% EtOAc/heptane) to give the title compound (302 mg, 91%) as an off-white solid. δH (CDCl3) 7.25-7.41 (5H, m), 7.02 (1H, d, J 9.0 Hz), 6.55 (1H, d, J 9.0 Hz), 4.91 (1H, s), 4.60 (2H, d, J 5.8 Hz), 2.53 (3H, s). LCMS (ES+) 200 (M+H)+, RT 2.50 minutes (Method 2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242116B2
出典データセットuspto-grants-2012_08
ORD IDord-97edd6a3912e4bb496eba53b2e8f2b55
出典メモuspto-grants-2012_08