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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218117Generated: October 26, 2026

3,4,5-Trimethoxybenzaldehyde → N-(2-Hydroxy-5-((1R,2S)-1-hydroxy-2-(3,4,5-trimethoxybenzylamino)propyl)phenyl)methane-sulfonamide

https://huagongshe.com/reaction/218117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantN-(5-((1R,2S)-2-Amino-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 58280635—
SolventMethanolHCID 887—
ProductN-(2-Hydroxy-5-((1R,2S)-1-hydroxy-2-(3,4,5-trimethoxybenzylamino)propyl)phenyl)methane-sulfonamideHCID 4462848336%

Reaction Steps

Borane-pyridine complex (135 μL, 1.28 mmol) was added to a methanol solution (4 mL) of an amine (3) (111 mg, 0.43 mmol) and 3,4,5-trimethoxybenzaldehyde (111 mg, 0.55 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 (7) as a white solid (67 mg, yield 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198330B2
Source datasetuspto-grants-2012_06
ORD IDord-9777778139064f1dbc92747cf093bb3a
Source noteuspto-grants-2012_06