HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (7S)-5-Azaspiro[2.4]heptan-7-amine--hydrogen chloride (1/2)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (S)-7-[(S)-1-Phenylethyl]amino-5-azaspiro[2.4]heptane | HCID 9920817 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Water | HCID 962 | — |
| Product | (7S)-5-Azaspiro[2.4]heptan-7-amine--hydrogen chloride (1/2) | HCID 23539486 | 82% |
Reaction Steps
An autoclave was charged with 79 mg of (S)-7-[(S)-1-phenylethyl]amino-5-azaspiro[2.4]heptane, 37 mg of 20% palladium hydroxide, 2 ml of ethanol, 1 ml of water and 0.5 ml of concentrated hydrochloric acid, and the contents were stirred overnight at room temperature in an atmosphere of hydrogen (40 kgf/cm2). After completion of the reaction, the catalyst was removed by filtration and the resulting filtrate was concentrated under a reduced pressure to obtain 72 mg (82%) of the title compound in the form of colorless crystals. The thus obtained crystal compound was recrystallized from ethanol and diethyl ether and used as a sample for analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218548B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-251950c2e3284c4fabc0c09cdfbb6eef |
| Source note | uspto-grants-2001_04 |