HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl [6-(2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl)-1h-benzimidazol-2-yl]carbamate dihydrochloride salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,1-dimethylethyl 7-(2-{[(methyloxy)carbonyl]amino}-1H-benzimidazol-6-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate | HCID 67515097 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl [6-(2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl)-1h-benzimidazol-2-yl]carbamate dihydrochloride salt | HCID 86672024 | 95% |
Reaction Steps
1,1-Dimethylethyl 7-(2-{[(methyloxy)carbonyl]amino}-1H-benzimidazol-6-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (517 mg, 1.18 mmol) was taken into methanol (2 mL) and 4M hydrogen chloride in dioxane (2 mL) and the mixture was allowed to stand at room temperature for 30 minutes. The suspension obtained was diluted with excess ethyl ether and the solid collected by filtration to give methyl [6-(2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl)-1H-benzimidazol-2-yl]carbamate dihydrochloride salt (462 mg, 95% yield) as a white solid. MS (EI) for C18H18N4O3: 339 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637499B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-95a8ac83d9ad4a8aaf5e80779ea947a1 |
| Source note | uspto-grants-2014_01 |