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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395852Generated: October 27, 2026

Toluene → N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide

https://huagongshe.com/reaction/395852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantMethanesulfonic AcidHCID 6395—
ReactantQuinolineHCID 7047—
Reactant2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
Reactant1-(Pyridin-4-yl)piperidin-4-olHCID 23447619—
SolventDichloromethaneHCID 6344—
ProductN-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamideHCID 1817441846%

Reaction Steps

To a mixture of 1-(4-pyridyl)-4-hydroxypiperidine (536 mg, 3.01 mmol) and methylene chloride (45 mL) was added methanesulfonic acid (0.2 ml, 3.1 mmol). After stirring for 15 seconds, quinoline (0.45 mL, 3.8 mmol) was added, immediately followed by 1.93 M phosgene in toluene (2 mL, 3.9 mmol). After 5 minutes, the reaction was placed in a 35° C. oil bath for 45 minutes. The reaction was cooled to room temperature and N-(4-methoxyphenyl)-2-aminobenzamide (728 mg, 3.0 mmol) and quinoline(0.45 mL, 3.8 mmol) were added. After stirring overnight, the reaction was diluted with CH2Cl2(150 mL) and washed with sat'd sodium carbonate (2×25 mL). The organic layer was concentrated and the crude residue was chromatographed to give 617 mg (46%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605626B2
Source datasetuspto-grants-2003_08
ORD IDord-2df88400879e4876b1fd1e7676a166ee
Source noteuspto-grants-2003_08