HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic-formic anhydride → HCID 18449084, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Reactant | HCID 10177192 | HCID 10177192 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18449084 | HCID 18449084 | — |
Reaction Steps
10-(4-Cyclohexyl-benzoyl)-10,11-dihydro-5H-pyrrolo[2,1-c][1.4]benzodiazepine of Example 4 (1.065 g) in dichloromethane (50 mL) was reacted with formic acetic anhydride. After stirring at room temperature overnight, the reaction mixture was washed with water and saturated aqueous sodium bicabonate, dried over anhydrous sodium sulfate and evaporated to dryness. The residue was filtered through a short column of Magnesol® to provide the desired title compound which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202239B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-73941a7883c849c190ae86f85b042d20 |
| Source note | uspto-grants-2007_04 |