Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594662Generated: November 4, 2026

p-Toluenesulfonic acid → HCID 69084124, compound

https://huagongshe.com/reaction/594662

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTriethyl orthoacetateHCID 66221—
ReactantHCID 69081808HCID 69081808—
SolventEthyl AcetateHCID 8857—
ProductHCID 69084124HCID 69084124—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-(3-amino-2-hydroxy-6-methoxyphenyl)-1-(quinolin-2-ylmethyl)piperidin-2-one (100 mg; 0.26 mmol), commercially available p-TsOH (2 mg; 0.01 mmol), and commercially available triethyl orthoacetate (290 mg; 1.69 mmol) was refluxed (100° C.) for 25 min. After cooling to rt, AcOEt was added, and the obtained mixture was filtered over a pad of celite. The filtrate was then washed with water and brine, and the mixed aq. layers were further extracted with AcOEt. The mixed organic layers were then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Subsequent purification by FC (DCM/MeOH=20/1) afforded the target compound. LC-MS (conditions A): tR=0.54 min.; [M+H]+: 401.73 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-4a12fcf9d4444a1cbf5b2488aa70fb8f
Source noteuspto-grants-2016_01