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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 218116Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/218116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-DichlorobenzaldehydeHCID 35746—
EduktN-(5-((1R,2S)-2-Amino-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 58280635—
LösungsmittelMethanolHCID 887—
ProduktN-(5-((1R,2S)-2-(3,5-Dichlorobenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 4462840945,3%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198330B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-e3b879a3c8494c3ca8d3a798a761c9df
Quellennotizuspto-grants-2012_06