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HRID 218118作成日:2026年10月23日

Benzaldehyde, 3,5-dimethyl- → N-(5-((1R,2S)-2-(3,5-Dimethylbenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamide

https://huagongshe.com/ja/reaction/218118

反応式

関与物質

役割名称HCID仕込み量
反応物Benzaldehyde, 3,5-dimethyl-HCID 34225—
反応物N-(5-((1R,2S)-2-Amino-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 58280635—
溶媒MethanolHCID 887—
生成物N-(5-((1R,2S)-2-(3,5-Dimethylbenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 4462848433%

反応手順

Borane-pyridine complex (160 μL, 1.50 mmol) was added to a methanol solution (5 mL) of an amine (3) (131 mg, 0.50 mmol) and 3,5-dimethylbenzaldehyde (90 μL, 0.65 mmol) at 40° C. and the mixture was stirred for 1.5 hours. The reaction mixture was allowed to cool to room temperature and extracted after addition of water with a mixed solvent (ethyl acetate: methanol=10:1), and the organic layer was washed with saturated aqueous sodium chloride solution. The organic layer was dried and concentrated, and the crude product obtained was purified by amine silica gel column chromatography (eluant:chloroform:methanol=7:1), to give a desired amine (8) as a white solid (62 mg, yield 33%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198330B2
出典データセットuspto-grants-2012_06
ORD IDord-f6b63811fd6c4cf3b29ec7d1f9687130
出典メモuspto-grants-2012_06