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HRID 1078070作成日:2026年10月25日

Sodium Hydroxide → (+-)-N-(cyclopropylmethyl)-1,2,3,4-tetrahydro-8-methoxy-2-naphthalenamine hydrochloride

https://huagongshe.com/reaction/1078070

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Sodium AcetateHCID 517045—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物8-Methoxy-3,4-dihydronaphthalen-1(2H)-oneHCID 11275335—
反応物N-methylcyclopropanamine hydrochlorideHCID 18546974—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒MeOH tetrahydrofuranHCID 21899815—
生成物(+-)-N-(cyclopropylmethyl)-1,2,3,4-tetrahydro-8-methoxy-2-naphthalenamine hydrochlorideHCID 18331788—

反応手順

To a solution of 2.64 g (15 mmol) 8-methoxy tetralone, 6 g (60 mmol) methylcyclopropylamine HCl and 4.92 g (60 mmol) NaOAc in 30 mL MeOH/THF (1:1) was added HOAc dropwise to adjust the pH to 4-5. The reaction mixture stirred for 15 minutes under N2, then 1.26 g (20 mmol) NaCNBH3 was added. When the reaction was complete by TLC (24 h), 1N NaOH (20 mL) and H2O (200mL) was added to quench the reaction. The solution was extracted with CH2Cl2 (2×500 mL) and the combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The resulting oil was purified by liquid chromatography on 400 g of silica gel 60 (230-400m), eluting with hexane/acetone (3:1). Fractions homogeneous by TLC were combined and concentrated in vacuo to give pure compound as an oil. The HCl salt was formed by using a MeOH/HCl solution. The title compound was recovered by recrystallization as a white solid using EtOAc/MeOH (1.77 g, 44%); m.p. 216°-218° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05545755
出典データセットuspto-grants-1996_08
ORD IDord-0befaaf73ea74a969b2dcb92bf7f6f38
出典メモuspto-grants-1996_08