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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207595Generated: November 1, 2026

Triethylamine → HCID 89649339, compound

https://huagongshe.com/reaction/2207595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl vinyl sulfoneHCID 79664—
ReactantMethanesulfonic acid, 1,1,1-trifluoro-, calcium salt (2:1)HCID 2734307—
Reactant3-Amino-1-methylpyrrolidin-2-oneHCID 45791133—
Reactant4-Bromo-3-methyl-2-pyridinecarboxaldehydeHCID 72209950—
SolventMethanolHCID 887—
ProductHCID 89649339HCID 8964933926.5%

Reaction Steps

To a stirred solution of 3-amino-1-methyl-pyrrolidin-2-one (3258.49 mg, 28.55 mmol) in methanol (8 mL) was added 4-bromo-3-methyl-pyridine-2-carbaldehyde (which may be prepared as described in Description 7) (5710 mg, 28.55 mmol), phenyl vinyl sulfone (4801.68 mg, 28.55 mmol), and calcium triflate (482.74 mg, 1.43 mmol). The reaction was stirred for 5 minutes. Triethylamine (3.97 mL, 28.55 mmol) was then added [caution—slight exotherm observed], and the reaction was stirred for 15 minutes. A large amount of solid was observed to precipitate out of the reaction, this was sonicated and stirred for a further 15 minutes. The solid was then filtered off, and washed with additional methanol (approximately 10 mL). The pale cream solid was then washed with diethyl ether (10 mL), and air dried for 10 minutes to give a colourless solid, then dissolved in MeOH (8 mL), and treated with phenyl vinyl sulfone (4801.68 mg, 28.55 mmol), calcium triflate (482.74 mg, 1.43 mmol) and lastly triethylamine (3.97 mL, 28.55 mmol). The reaction mixture was then stirred at room temperature for 16 hours. The solid was filtered off, and washed with Et2O (10 mL). The solid was then air dried for 15 minutes on the sinter to afford 7-(benzene-sulfonyl)-8-(4-bromo-3-methyl-2-pyridyl)-3-methyl-3,9-diazaspiro[4.4]nonan-4-one (D8) (3520 mg, 7.58 mmol, 26.5% yield);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376436B2
Source datasetuspto-grants-2016_06
ORD IDord-5a1b1219504f44fc84ffcc9b60000c27
Source noteuspto-grants-2016_06