HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 9-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1-Dimethylethyl 9-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate | HCID 59403490 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 9-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride | HCID 68465494 | 129.6% |
Reaction Steps
1,1-Dimethylethyl 9-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (Preparation 66) (320 mg, 0.658 mmol) was dissolved in 1,4-dioxane (1 ml) and treated with HCl (2 ml, 8.00 mmol) in 1,4-dioxane. The reaction mixture was left at RT for 1 hr, evaporated and then triturated with ether to give the title compound (180 mg) as a white solid. MS (ES): C20H2035ClN3O3 requires 385; found 386 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222245B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-28ff002950a24d4a834b4c74787ca79c |
| Source note | uspto-grants-2012_07 |