HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicarbonate Ion → methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-bromobutyrate | HCID 107604 | — |
| Reactant | hexahydro-1-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine | HCID 11197238 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-butanoate | HCID 68489685 | 79.7% |
Reaction Steps
In a manner similar as described above in Paragraph A, a solution of hexahydro-1-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine (150 mg, 0.506 mmol) and methyl 4-bromobutanoate (0.29 mL, 2.0 mmol) in THF (6 mL) was treated with triethylamine (0.28 mL, 2 mmol) and the reaction was heated at reflux for 4 hours. The reaction was allowed to cool and treated with an aqueous bicarbonate solution. The combined ethyl acetate extracts were washed with water, dried and concentrated to give 0.16 g of methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-butanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737145B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bb0e708cf4c14bd1beb626c6497cc125 |
| Source note | uspto-grants-2010_06 |