HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5-Trimethoxybenzaldehyde → N-(2-Hydroxy-5-((1R,2S)-1-hydroxy-2-(3,4,5-trimethoxybenzylamino)propyl)phenyl)methane-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | N-(5-((1R,2S)-2-Amino-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamide | HCID 58280635 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-Hydroxy-5-((1R,2S)-1-hydroxy-2-(3,4,5-trimethoxybenzylamino)propyl)phenyl)methane-sulfonamide | HCID 44628483 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198330B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-9777778139064f1dbc92747cf093bb3a |
| Source note | uspto-grants-2012_06 |