HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67165613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2S)-2-amino-4-(methylsulfanyl)butanamide hydrochloride | HCID 18531008 | — |
| Reactant | HCID 24710387 | HCID 24710387 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67165613 | HCID 67165613 | — |
Reaction Steps
A solution of 1-(2-ethylbutyryl)-piperidin-4-one (1.6 g, 8.1 mmol), (S)-methioninamide hydrochloride (1.5 g, 8.1 mmol), and triethylamine (820 mg, 8.1 mmol) in EtOH (66 mL) was heated under reflux over a period of 16 h. Following removal of the solvent, water (50 mL) and CH2Cl2 (50 mL) were added to the residue and the mixture was basified with concentrated sodium hydroxide solution. The aqueous phase was extracted with CH2Cl2 (3×20 mL) and the combined organic phases were dried over Na2SO4. Following removal of the solvent and vacuum drying, there was obtained the product 8-(2-ethylbutyryl)-3-(S)-(2-methylsulfanylethyl)-1,4,8-triazaspiro[4,5-]-decan-2-one in a yield of 1.8 g (69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951815B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-46cdc0a7f95b4ffdabf30cb12392801d |
| Source note | uspto-grants-2011_05 |