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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883012Generated: October 25, 2026

Cycloheptanone → 5-Chloro-N-(5-methylpyridin-2-yl)-2-[(1-cycloheptylpiperidin-4-yl)methylamino]benzamide

https://huagongshe.com/reaction/1883012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloheptanoneHCID 10400—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamideHCID 21906309—
SolventTetrahydrofuranHCID 8028—
SolventAcetic acid methanolHCID 10129899—
Product5-Chloro-N-(5-methylpyridin-2-yl)-2-[(1-cycloheptylpiperidin-4-yl)methylamino]benzamideHCID 2190654072.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 5-chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide from Example 99-A (0.45 g, 1.25 mmol) in 10 mL of 95:5 methanol-acetic acid was treated with excess cycloheptanone (1.48 mL, 12.5 mmol), followed by sodium cyanoborohydride (5.0 ml of a 1 M solution in tetrahydrofuran, 6.0 mmol). After stirring at 50° C. for 96 h, the mixture was concentrated in vacuo; and the residue was subjected to silica gel chromatography. Elution with 9:1 dichloromethane-methanol provided 0.41 g (72%) of the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759414B2
Source datasetuspto-grants-2004_07
ORD IDord-cc3df80f78ad4962a856553c342e321f
Source noteuspto-grants-2004_07