HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 7-[(acetoxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]8,9-dihydro-10-methylpyrido[1,2-a]indol-6(7H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 8,9-dihydro-7-[(hydroxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]-10-methylpyrido[1,2-a]indol-6(7H)-one | HCID 15051923 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 7-[(acetoxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]8,9-dihydro-10-methylpyrido[1,2-a]indol-6(7H)-one | HCID 10416056 | — |
Reaction Steps
Acetic anhydride (5 ml) was added to a solution of 8,9-dihydro-7-[(hydroxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]-10-methylpyrido[1,2-a]indol-6(7H)-one (4 g, a mixture of the isomers A and B) in pyridine (50 ml). After being stirred at room temperature for 20 hours, the solution was evaporated in vacuo. Silica gel column chromatography (1% methanol-methylene chloride) of the oil obtained gave 7-[(acetoxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]8,9-dihydro-10-methylpyrido[1,2-a]indol-6(7H)-one (4.30 g) as an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05290785 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-20152ff630b440d9ae5c2bc9a9ac50ba |
| Source note | uspto-grants-1994_03 |