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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914937Generated: October 30, 2026

3-Iodotoluene → Rac-4-phenyl-8-(1-m-tolyl-cyclohexyl)-2,8-diaza-spiro[4.5]decan-1-one

https://huagongshe.com/reaction/914937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-IodotolueneHCID 12268—
ReactantRac-1-(1-oxo-4-phenyl-2,8-diaza-spiro [4.5]dec-8-yl)-cyclohexanecarbonitrileHCID 69486548—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductRac-4-phenyl-8-(1-m-tolyl-cyclohexyl)-2,8-diaza-spiro[4.5]decan-1-oneHCID 1137304171%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-iodotoluene (388 mg, 1.8 mmol) in dry THF (6 mL) under argon at -60° C. was added isopropylmagnesium chloride (2 M solution in THF, 977 μL, 2.0 mmol) and the resulting solution allowed to warm up to 0° C. over 1 h and then to room temperature over 10 min. The resulting solution was then added dropwise to a solution of rac-1-(1-oxo-4-phenyl-2,8-diaza-spiro[4.5]dec-8-yl)-cyclohexanecarbonitrile (200 mg, 0.6 mmol) in dry THF (3 mL) and the solution stirred overnight at room temperature. The reaction was quenched by the addition of ammonium chloride solution (sat., 10 mL) and the product extracted with ethyl acetate (2×20 mL). The combined organic extracts were then washed with brine (20 mL), dried over sodium sulfate, filtered and evaporated. The residue was purified by chromatography on silica gel eluting with DCM:MeOH:NH4OH (95:4.5:0.5) to afford the title compound (170 mg, 71%) as a white solid. MS: m/e=403.6 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265126B2
Source datasetuspto-grants-2007_09
ORD IDord-92db3e2d0d5d4ccc98a7ef3095417625
Source noteuspto-grants-2007_09