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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552330Generated: October 26, 2026

Triethylamine → HCID 67165786, compound

https://huagongshe.com/reaction/552330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(2S)-2-amino-4-(methylsulfanyl)butanamide hydrochlorideHCID 18531008—
ReactantHCID 24695582HCID 24695582—
SolventEthanolHCID 702—
ProductHCID 67165786HCID 67165786—

Reaction Steps

A solution of 1-(2,4-dimethoxybenzoyl)piperidin-4-one (1.4 g, 5.1 mmol), (S)-methioninamide hydrochloride (950 mg, 5.1 mmol) and triethylamine (520 mg, 5.1 mmol) in EtOH (40 ml) was heated under reflux for 2.5 h and stirred at RT for a further 16 h. After removal of the solvent, water (25 ml) and CH2Cl2 (25 ml) were added to the residue and it was rendered basic using conc. sodium hydroxide solution. The aqueous phase was extracted with CH2Cl2 (3×20 ml) and the combined organic phases were dried over Na2SO4. After removal of the solvent and drying in vacuo, the product 8-(2,4-dimethoxybenzoyl)-3-(S)-(2-methylsulfanylethyl)-1,4,8-triazaspiro[4,5]decan-2-one was obtained in a yield of 1.9 g (95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-db89d749cab048ac8f8e678926939213
Source noteuspto-grants-2011_05