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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098299Generated: October 30, 2026

Methyl iodide → HCID 23156895, compound

https://huagongshe.com/reaction/1098299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantHCID 23156875HCID 23156875—
SolventAcetonitrileHCID 6342—
ProductHCID 23156895HCID 2315689548.3%

Reaction Steps

0.0185 ml (0.133 mmol) of triethylamine and 0.00665 ml (0.107 mmol) of iodomethane were added to an acetonitrile solution (0.4 ml) containing 3.6 mg (0.0089 mmol) of the 7-(3-hydroxypiperidin-1-yl)-3-(2-piperazin-1-ylphenyl)-2H-isoquinolin-1-one obtained in Example 102. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, the solvent was distilled away under reduced pressure. The obtained residue was developed and purified by thin-layer chromatography (NH2 F254s, Merck, developing solvent; dichloromethane:methanol=10:1, Rf value: 0.8), so as to obtain 1.8 mg (48%) of 7-(3-hydroxypiperidin-1-yl)-3-[2-(4-methylpiperazin-1-yl)phenyl]-2H-isoquinolin-1-one in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143274B2
Source datasetuspto-grants-2012_03
ORD IDord-6dd423511a8e48a6a2723c1faec61b98
Source noteuspto-grants-2012_03