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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101434Generated: October 30, 2026

Benzoic Acid → 4-Isopropylamino-1-(4-methoxypyrid-3-ylmethyl)piperidine monobenzoic acid salt

https://huagongshe.com/reaction/2101434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantN-isopropyl-1-((4-methoxypyridin-3-yl)methyl)piperidin-4-amineHCID 11651846—
Solventtert-Butyl methyl etherHCID 15413—
Product4-Isopropylamino-1-(4-methoxypyrid-3-ylmethyl)piperidine monobenzoic acid saltHCID 6742746782.9%

Reaction Steps

Benzoic acid (1451 g, 11.9 mol) and MTBE (5.8 L) were added to a 50 L 3-necked round-bottom flask equipped with a mechanical stirrer, thermometer, nitrogen inlet and heating mantle. The resulting slurry was heated at 45° C. to 50° C. to dissolve the benzoic acid. A solution of 4-isopropylamino-1-(4-methoxypyrid-3-ylmethyl)piperidine (3130 g, 11.9 mol) in methy tert-butyl ether (MTBE) (13.7 L) was added at 45° C. to 50° C. and the resulting mixture was stirred at reflux (50° C. to 55° C.) for 30 minutes and then at ambient temperature for 16 hours. The reaction mixture was then cooled to 0° C. to 5° C. with an ice/methanol bath and stirred for 30 minutes at which time a solid had formed. The solid was filtered through a polypropylene filter pad and washed with MTBE (3×2 L) and ethyl ether (3×2 L). The solid was then tray dried in a vacuum oven at room temperature until a constant weight was obtained to provide the title compound (3805 g, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572918B2
Source datasetuspto-grants-2009_08
ORD IDord-413feeb9313e49baa6aa83e5bb789c56
Source noteuspto-grants-2009_08