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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425750Generated: October 30, 2026

Water → HCID 59822474, compound

https://huagongshe.com/reaction/2425750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 4-(iodomethyl)piperidine-1-carboxylateHCID 10448961—
ReactantHCID 59822470HCID 59822470—
SolventDimethylformamideHCID 6228—
ProductHCID 59822474HCID 5982247432.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-isopropyl-5-methyl-2-oxo-N-(piperidin-4-ylmethyl)-1,2-dihydroquinoline-3-carboxamide (300 mg, 0.88 mmol, step 4 in preparation 3) in N,N-dimethylformamide (30 mL), tert-butyl 4-(iodomethyl)piperidine-1-caroxylate (343 mg, 1.05 mmol, Villalobos Anabella et al., J. Med. Chem., 1994, 37, 2721) and potassium carbonate (610 mg, 4.4 mmol) were added at room temperature. The mixture was heated at 80° C. overnight. After cooled to room temperature, water (30 mL) was added and extracted with diethyl ether (50 mL×2). The combined organic layer was washed with water (20 mL×2), brine (20 mL), dried over magnesium sulfate and concentrated in vacuo gave yellow oil, which was chromatographed on a column of silica gel eluting with ethyl 25% ammonium oxide/methanol/dichloromethane (3:30:1000) to give 154 mg (32%) of the title compound as a clear colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964727B2
Source datasetuspto-grants-2011_06
ORD IDord-780eeeb820544fabb86f77dd04e9143f
Source noteuspto-grants-2011_06