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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227256Generated: October 30, 2026

Triethylamine → 1,3-Dibenzyl-8-methanesulfonyl-1,4,8-triazaspiro[4,5]decan-2-one

https://huagongshe.com/reaction/227256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,3-Dibenzyl-1,4,8-triazaspiro[4,5]decan-2-oneHCID 68837942—
SolventDichloromethaneHCID 6344—
Product1,3-Dibenzyl-8-methanesulfonyl-1,4,8-triazaspiro[4,5]decan-2-oneHCID 68837760—

Reaction Steps

Triethylamine (0.15 ml, 1.78 mmol) and subsequently methanesulfonyl chloride (0.14 ml, 1.78 mmol) were added to a solution of 1,3-dibenzyl-1,4,8-triazaspiro-[4,5]decan-2-one (300 mg, 0.89 mmol) in CH2Cl2 (8.1 ml) with stirring using nitrogen as an inert gas at RT. The reaction mixture was stirred overnight. The organic phase was rendered alkaline using aqueous sodium carbonate solution (20 ml) and the aqueous phase was extracted with CH2Cl2 (15 ml). The combined organic phases were dried over Na2SO4. After filtration, removal of the solvent, and column chromatography, the desired product 1,3-dibenzyl-8-methanesulfonyl-1,4,8-triazaspiro[4,5]decan-2-one was obtained in a yield of 287 mg (77% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560468B2
Source datasetuspto-grants-2009_07
ORD IDord-7c42931adaa44c64920a7af1ef5adef0
Source noteuspto-grants-2009_07