HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 7-Benzylamino-4-oxo-5-azaspiro[2.4]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-(1-Benzylamino-1-cyanomethyl)-1-ethoxycarbonylcyclopropane | HCID 15391046 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | 7-Benzylamino-4-oxo-5-azaspiro[2.4]heptane | HCID 15429261 | — |
Reaction Steps
An autoclave was charged with 61.3 mg of 1-(1-benzylamino-1-cyanomethyl)-1-ethoxycarbonylcyclopropane, 0.2 ml of Raney nickel and 2.0 ml of ammonia-saturated ethanol, and the contents were stirred at room temperature for 2 hours in an atmosphere of hydrogen under a pressure of 30 kg/cm2. After completion of the reaction, the catalyst was removed by filtration and the resulting filtrate was concentrated under a reduced pressure to obtain 51.3 mg (quantitative) of the title compound in the form of light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218548B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-1b78b40bb35e4dea8b8e9d3cf0420990 |
| Source note | uspto-grants-2001_04 |