戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 218116作成日:2026年10月26日

3,5-Dichlorobenzaldehyde → N-(5-((1R,2S)-2-(3,5-Dichlorobenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamide

https://huagongshe.com/reaction/218116

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DichlorobenzaldehydeHCID 35746—
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-Dichlorobenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 4462840945.3%

反応手順

Borane-pyridine complex (130 μL, 1.21 mmol) was added to an methanol solution (4 mL) of an amine (3) (105 mg, 0.40 mmol) and 3,5-dichlorobenzaldehyde (95 mg, 0.52 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 (6) as a white solid (76 mg, yield 45%).

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-e3b879a3c8494c3ca8d3a798a761c9df
出典メモuspto-grants-2012_06