Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685899Generated: November 1, 2026

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

https://huagongshe.com/reaction/1685899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
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

To a solution of the amine (4) (111 mg, 0.43 mmol) and 3,4,5-trimethoxybenzaldehyde (111 mg, 0.55 mmol) in methanol (4 mL) was added borane-pyridine complex (135 μL, 1.28 mmol) at 40° C. and the resulting mixture was stirred for 1.5 hours. The reaction mixture was cooled to room temperature and water was added thereto, followed by extraction with a mixed solvent (ethyl acetate:methanol=10:1) and subsequent washing of the organic layer with saturated brine. The organic layer was dried and concentrated and the obtained crude product was purified by amine silica gel column chromatography (eluent; chloroform:methanol=7:1) to obtain the desired amine (8) as a white solid (67 mg, Yield: 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148427B2
Source datasetuspto-grants-2012_04
ORD IDord-a3266e0b1e004f3cb591b9cd15d481b6
Source noteuspto-grants-2012_04