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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157452Generated: November 3, 2026

p-Anisoyl chloride → HCID 17611455, compound

https://huagongshe.com/reaction/1157452

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantPiperidine-1-propylamineHCID 19049—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductHCID 17611455HCID 1761145569%

Reaction Steps

To a solution of N-3-aminopropylpiperidine (1.4 g, 10 mmol) in dichloromethane (20 mL) was added DIEA (1.9 mL, 11 mmol) followed by slow addition of 4-methoxy benzoyl chloride (1.9 g, 11 mmol). The reaction mixture was stirred at room temperature for 18 h. The solution was washed with 1 N KOH (aq.) (1×20 mL) and brine (1×20 mL). The organic phase was dried (K2CO3) and concentrated in vacuo to afford 4-methoxy-N-(3-piperidin-1-ylpropyl)benzamide (1.9 g, 6.9 mmol, 69%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807686B2
Source datasetuspto-grants-2010_10
ORD IDord-5188b15100504a899bed7c42c702f7b8
Source noteuspto-grants-2010_10