HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(2-Isopropyl-5-methyl-1,2,4-triazol-3-yl)-9-[2-(3-piperidyl)pyrazol-3-yl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 9-(1-(1-benzylpiperidin-3-yl)-1H-pyrazol-5-yl)-2-(1-isopropyl-3-methyl-1H-1,2,4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine | HCID 68313179 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Isopropyl-5-methyl-1,2,4-triazol-3-yl)-9-[2-(3-piperidyl)pyrazol-3-yl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine | HCID 68313001 | — |
Reaction Steps
9-(1-(1-benzylpiperidin-3-yl)-1H-pyrazol-5-yl)-2-(1-isopropyl-3-methyl-1H-1,2,4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine (500 mg, 0.0009 mol) was dissolved in Methanol (10 mL). 4.0 M of Hydrogen chloride in 1,4-Dioxane (0.5 mL, 0.002 mol) was added. 10% Palladium on Carbon (0.1:0.9, Palladium: carbon black, 120 mg, 0.00011 mol) was added under a stream of Nitrogen. The reaction mixture was vac/flushed with H2 (balloon) and stirred overnight at room temperature. LCMS show reaction is complete. The reaction mixture was filtered and concentrated to dryness to give 2-(1-isopropyl-3-methyl-1H-1,2,4-triazol-5-yl)-9-(1-(piperidin-3-yl)-1H-pyrazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090628B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-4f32a797b75a4c4b80fb26212c7c3804 |
| Source note | uspto-grants-2015_07 |