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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797892Generated: November 4, 2026

4-Methylpiperidine → HCID 25128215, compound

https://huagongshe.com/reaction/1797892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpiperidineHCID 69381—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantHCID 178515184HCID 178515184—
SolventDichloromethaneHCID 6344—
ProductHCID 25128215HCID 25128215—

Reaction Steps

A solution of 2-phenyl-2,5-dihydro-pyrazolo-(4,3-c)quinolin-3-one (4a) (0.261 g, 1 mM) in 2 mL of anhydrous methylene chloride was stirred with N,N-diisopropylethylamine (0.145 g, 1.2 mM) and triphosgene (0.173 g, 0.55 mM) at 0° C. for 1 hour and 25° C. for 2 hours. N,N-diisopropylethylamine (0.145 g, 1.2 mM) and 4-methylpiperidine (0.208 g, 2 mM) were added at 0° C. and the reaction mixture was stirred overnight at room temperature. The reaction was quenched by addition of aqueous sodium bicarbonate solution. The organic layer was collected, washed with brine solution, dried over sodium sulfate, filtered and concentrated in vacuo. The product was obtained by column chromatography. 1H NMR (CDCl3) δ (ppm): 1.0 (3H, d, J=6.59), 1.6 (4H,m), 1.84 (1H,m), 3.14 (1H,m), 3.30 (1H,m), 4.01, (1H,m), 4.60 (1H,m), 7.20 (1H, t, J=8.57), 7.38 (1H, m), 7.68-7.42 (4H, m), 8.18 (2H, m), 8.28 (1H, s), 8.44 (1H, d, J=8.81 Hz). m/z 387.5 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343957B2
Source datasetuspto-grants-2013_01
ORD IDord-335de1aa63be473a9a47bdcf0d915a1c
Source noteuspto-grants-2013_01