HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen chloride-ethyl acetate → hexahydro-1,1-diphenyl-1H-oxazolo[3,4-a][1,4]diazepin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | 1,1-Dimethylethyl tetrahydro-3-oxo-1,1-diphenyl-1H-[1,3]oxazolo[3,4-a][1,4]diazepine-8(5H)-carboxylate | HCID 23121874 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | hexahydro-1,1-diphenyl-1H-oxazolo[3,4-a][1,4]diazepin-3-one | HCID 23122043 | 71.1% |
Reaction Steps
1,1-Dimethylethyl tetrahydro-3-oxo-1,1-diphenyl-1H-[1,3]oxazolo[3,4-a][1,4]diazepine-8(5H)-carboxylate (0.30 g, 0.73 mmol) was dissolved in ethyl acetate (5 mL). A 4 M hydrogen chloride/ethyl acetate solution (4 mL) was added thereto, and the mixture was stirred at room temperature for 1 hour. The reaction solution was concentrated, and then ethyl acetate was added to the residue. The resulting mixture was washed with a 0.5 M aqueous sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain the title compound (0.16 g, yield 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795267B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-2e504ad419b342ee845279880f7d8961 |
| Source note | uspto-grants-2010_09 |