Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stearoyl chloride | HCID 8212 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22013764 | HCID 22013764 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 9849308 | HCID 9849308 | 86.1% |
Reaction Steps
Triethylamine (1.46 ml) was added to a solution containing 3-amino-4-{[3-(dimethylamino)propyl]amino}-N,N-dimethylbenzamide (2.57 g) in chloroform (20 ml), and then stearoyl chloride (2.89 g) was added thereto while being cooled with ice. After being stirred for 2 hours at room temperature, the reaction mixture was diluted with chloroform, washed with saturated sodium hydrogencarbonate aqueous solution and water successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (7.5 ml) was added to a solution containing the residue (5.53 g) in ethanol (30 ml). After being stirred for 3 hours at 90° C., the reaction mixture was neutralized with 5N sodium hydroxide aqueous solution (18 ml) and concentrated. The residue, with ethyl acetate added thereto, was washed with water and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The residue (4.33 g) was purified by silica gel column chromatography (silica gel 50 g, chloroform:methanol=10:1), thereby yielding the entitled compound (4.21 g) as pink wax.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06204264B1 |
|---|
| Source dataset | uspto-grants-2001_03 |
|---|
| ORD ID | ord-0e9887e2adfa44f9b41a147a919fd199 |
|---|
| Source note | uspto-grants-2001_03 |
|---|