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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294574Generated: October 25, 2026

Methylamine ethanol → 8-[2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-3-(3-methylamino-propyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

https://huagongshe.com/reaction/1294574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamine ethanolHCID 22028356—
Reactant3-(3-Chloro-propyl)-8-[2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-oneHCID 58906443—
CatalystSodium IodideHCID 5238—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product8-[2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-3-(3-methylamino-propyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-oneHCID 1123633752.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

The crude spiro compound (23) (162.8 g; 0.36 mol) was dissolved in methylamine/EtOH solution (Fluka, 8M; 1154 ml; 9.23 mol). Sodium iodide (2.16 g; 0.014 mol) was added and the solution was stirred at 70° C. under N2-atmosphere for 3 days. After cooling the reaction mixture was diluted with water and EtOAc (500 ml each). The aqueous layer was extracted with EtOAc (3×800 ml). The organic layer was washed with brine (500 ml). After drying on Na2SO4 the solvent was evaporated to yield a yellow oil. This oil was purified by column chromatography (SiO2; CH2Cl2/MeOH 90:10; containing 1% 7N NH3/MeOH) to yield 30 g of (24) with a purity of 93% (according to HPLC/MS) and 85 g of (24) with a purity of 96% (115 g; 0.25 mol; 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241770B2
Source datasetuspto-grants-2007_07
ORD IDord-9cab9986065f42eb9aadb90d095cd1d8
Source noteuspto-grants-2007_07