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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271616Generated: November 3, 2026

Triethylamine → 1-methanesulfonyl-N-(1-phenyl-4-piperidyl)spiro[indoline-3,4'-piperidine]-1'-carboxamide

https://huagongshe.com/reaction/1271616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Methylsulfonyl)spiro[indoline-3,4'-piperidine] hydrochlorideHCID 21956084—
ReactantHCID 22936218HCID 22936218—
SolventChloroformHCID 6212—
Product1-methanesulfonyl-N-(1-phenyl-4-piperidyl)spiro[indoline-3,4'-piperidine]-1'-carboxamideHCID 2293622331.6%

Reaction Steps

1-Methanesulfonyl-spiro[indoline-3,4′-piperidine] hydrochloride (37 mg) and triethylamine (170 μL) were added to a solution of phenyl N-(1-phenyl-4-piperidyl)carbamate (36 mg) in chloroform (3 mL), and the mixture was heated to reflux for 15 hours. The reaction mixture was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was crystallized from diethyl ether to give the title compound (18 mg) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205417B2
Source datasetuspto-grants-2007_04
ORD IDord-36c83ac409744c73b3f00b96ca188e3e
Source noteuspto-grants-2007_04