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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249669Generated: October 29, 2026

4-Methylpiperidine → HCID 25128215, compound

https://huagongshe.com/reaction/249669

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 numberUS07863266B2
Source datasetuspto-grants-2011_01
ORD IDord-9c8a46a110e3453ba08d7aee2ec3793e
Source noteuspto-grants-2011_01