HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-Boc-9-Cbz-3-oxa-7,9-diazabicyclo[3.3.1]nonane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | tert-Butyl 3-oxa-7,9-diazabicyclo(3.3.1)nonane-7-carboxylate | HCID 53415349 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Boc-9-Cbz-3-oxa-7,9-diazabicyclo[3.3.1]nonane | HCID 117698100 | 80% |
Reaction Steps
To a solution of tert-butyl 3-oxa-7,9-diazabicyclo[3.3.1]nonane-7-carboxylate (0.500 g, 2.2 mmol) in dichloromethane (5 ml) was added triethylamine (0.443 g, 4.4 mmol) at room temperature. The mixture was stirred at room temperature for a few mins, and then benzyl chloroformate (0.751 g, 4.4 mmol) was added to the reaction mixture. The resulting mixture was stirred at room temperature overnight. The mixture was partitioned between dichloromethane and water. The organic phase was dried, and concentrated. The residue was purified by silica gel chromatography to give 9-benzyl 7-tert-butyl 3-oxa-7,9-diazabicyclo[3.3.1]nonane-7,9-dicarboxylate 133b (0.637 g, 80.0%). MS: calc'd (MH+) 363, measured (MH+) 363.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266904B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-f13193c56c164872b5c85dc6bc3ebf5e |
| Source note | uspto-grants-2016_02 |