HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20542090, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20542075 | HCID 20542075 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20542090 | HCID 20542090 | — |
Reaction Steps
A solution of 2.5 g (7.34 mmol) of 5-(o-fluorophenyl)-1,3-dihydro-7-(1-hydroxyethyl)-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one in 10 ml of acetic acid anhydride and 10 ml of pyridine is left to stand at room temperature for 24 hours and then concentrated in vacuo. The residue is taken up in chloroform and the organic phase is washed successively with 2 N hydrochloric acid, 2 N sodium bicarbonate solution and water, dried and evaporated. The residue is chromatographed on 50 g of silica gel using chloroform as the elution agent. There is obtained 1-[5-(o-fluorophenyl)-2,3-dihydro-1,3,3-trimethyl-2-oxo-1H-1,4-benzodiazepin-7-yl]ethyl acetate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04327026 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-d9087cb3f4c042dab20d7fb5e47859e0 |
| Source note | uspto-grants-1982_04 |