HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 8-amino-5-Azaspiro[3.5]nonane-5-carboxylic acid 1,1-dimethylethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-butyl 8-oxo-5-azaspiro[3.5]nonane-5-carboxylate | HCID 17435105 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 8-amino-5-Azaspiro[3.5]nonane-5-carboxylic acid 1,1-dimethylethyl ester | HCID 16228675 | — |
Reaction Steps
A of solution 8-Oxo-5-aza-spiro[3.5]nonane-5-carboxylic acid tert-butyl ester (Tetrahedron Letters 42, 4815 (2001)) (488 mg, 2.04 mmol) in 11 ml of MeOH was treated with ammonium acetate (1.5 g, 20.4 mmol) and sodium cyanoborohydride (100 mg, 1.6 mmol). This mixture was stirred at room temperature for 72 hours. Afterwards 0.8 ml 1N-HCl were added and stirring continued for 10 minutes. For extraction with EtOAc the solution was basified with 1N-NaOH. The crude was purified by chromatography on silicagel (DCM/MeOH/ammonia:9/1/0.1). Yield: 0.27 g (55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07615562B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-7f81cb2e876e4885a3c88b68317a8e04 |
| Source note | uspto-grants-2009_11 |