HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → N-(4-Benzyloxy-benzyl)-6-(ethoxymethyl-amino)-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 6-amino-N-(4-benzyloxy-benzyl)-nicotinamide | HCID 23130588 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-Benzyloxy-benzyl)-6-(ethoxymethyl-amino)-nicotinamide | HCID 23130644 | 40% |
Reaction Steps
To a solution of the resulting 6-amino-N-(4-benzyloxy-benzyl)-nicotinamide (200 mg, 0.556 mmol) in ethanol (10 mL) were added 5,5-dimethylimidazophospho-2,4-dione (85 mg, 0.66 mmol) and 37% formaldehyde aqueous solution (1 mL), and the solution was stirred for 1 hour under reflux. Water and ethyl acetate were added to the reaction solution, which was then partitioned, and the organic layer was washed twice. NH silica gel was added to the organic layer, the solvent was evaporated in vacuo for adsorption, purification was carried out by NH silica gel column chromatography (ethyl acetate), and the title compound (95 mg, 0.243 mmol, 40%) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932272B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-4ec199a9154a49beb42858092c722d04 |
| Source note | uspto-grants-2011_04 |