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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419435Generated: October 25, 2026

Water → Phenylmethyl 4-{1-[2-methyl-5-(methyloxy)-4-nitrophenyl]-4-piperidinyl}-1-piperazinecarboxylate

https://huagongshe.com/reaction/419435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-5-methoxy-2-methyl-4-nitrobenzeneHCID 18468141—
ReactantPhenylmethyl 4-(4-piperidinyl)-1-piperazinecarboxylate bis(trifluoroacetate) saltHCID 86625193—
SolventDimethyl SulfoxideHCID 679—
ProductPhenylmethyl 4-{1-[2-methyl-5-(methyloxy)-4-nitrophenyl]-4-piperidinyl}-1-piperazinecarboxylateHCID 5945295266%

Reaction Steps

5-Fluoro-4-methyl-2-nitrophenyl methyl ether (2.76 g, 14.9 mmol) was dissolved in DMSO (50 mL), and K2CO3 (10.3 g, 74.5 mmol) and phenylmethyl 4-(4-piperidinyl)-1-piperazinecarboxylate bis(trifluoroacetate) salt (Example 112, step B) (8.0 g, 15 mmol) were added. Reaction was stirred overnight. Poured into H2O and extracted (2×) with EtOAc. Combined organic layers were back-extracted (5×) with H2O and then dried over MgSO4, filtered, concentrated on to silica gel and flash chromatographed to give the title compound of step C (4.6 g, 66%). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.72 (s, 1H), 7.03-7.46 (m, 5H), 6.64 (s, 1H), 5.03 (s, 2H), 3.85 (s, 3H), 3.06-3.59 (m, 6H), 2.67 (t, J=11.5 Hz, 2H), 2.26-2.57 (m, 5H), 2.15 (s, 3H), 1.81 (d, J=11.5 Hz, 2H), 1.36-1.68 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-c7faefb670e74b6c9e032c4c44576cfe
Source noteuspto-grants-2012_01