HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → N-(5-benzylthiophen-2-ylmethyl)-6-(methoxymethyl-amino)-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Naphthylaminomethyl-gamma-aminobutyric acid | HCID 191061 | — |
| Reactant | 6-amino-N-(5-benzylthiophen-2-ylmethyl)-nicotinamide | HCID 23130353 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(5-benzylthiophen-2-ylmethyl)-6-(methoxymethyl-amino)-nicotinamide | HCID 23130744 | 87.6% |
Reaction Steps
To a solution of 6-amino-N-(5-benzylthiophen-2-ylmethyl)-nicotinamide described in Example A-144 (210 mg, 0.65 mmol) and 5,5-dimethylimidazo phospho-2,4-dione (92 mg, 0.71 mmol) in methanol (15 mL) was added an aqueous solution of 37% formaldehyde (2.5 mL) under reflux in three time, and the solution was stirred for 1 hour. NH silica gel was added to the reaction solution, the solvent was evaporated in vacuo for adsorption, purification was carried out by NH silica gel column chromatography (hexane:ethyl acetate=1:1, then ethyl acetate), and the title compound (210 mg, 0.57 mmol, 87.6%) 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-a07a50c3babf45bda94512c29e6abd41 |
| Source note | uspto-grants-2011_04 |