Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552335Generated: October 26, 2026

Triethylamine → HCID 67165613, compound

https://huagongshe.com/reaction/552335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(2S)-2-amino-4-(methylsulfanyl)butanamide hydrochlorideHCID 18531008—
ReactantHCID 24710387HCID 24710387—
SolventEthanolHCID 702—
ProductHCID 67165613HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-46cdc0a7f95b4ffdabf30cb12392801d
Source noteuspto-grants-2011_05