Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67747656 | HCID 67747656 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67748007 | HCID 67748007 | — |
Reaction Steps
A solution was 50 mg of the resultant compound of Example 185 and 20 mg of 10% Pd/C was stirred vigorously under a hydrogen atmosphere. After 30 minutes, the catalyst was filtered off and the filtrate concentrated to give a colorless oil, which was dissolved in 2 ml of CH2Cl2. The solution was cooled to 0° C., 0.03 ml of triethylamine and 0.01 ml of acetyl chloride were added. After 2 hrs, the solution was concentrated and the crude product purified by silica gel column chromatography (5% MeOH/CH2Cl2) to give 16 mg of the desired compound. Mass spectrum: (M+H)+ =565.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05545750 |
|---|
| Source dataset | uspto-grants-1996_08 |
|---|
| ORD ID | ord-afd0014b89484b16b190020a10f1fb34 |
|---|
| Source note | uspto-grants-1996_08 |
|---|