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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5741Generated: October 26, 2026

Methyl iodide → N-[2-(4-Chloro-N-methylcinnamylamino)ethyl]-5-isoquinolinesulfonamide

https://huagongshe.com/reaction/5741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 176156—
SolventChloroformHCID 6212—
ProductN-[2-(4-Chloro-N-methylcinnamylamino)ethyl]-5-isoquinolinesulfonamideHCID 53675817—

Reaction Steps

1.50 g of the product of Example 172 was dissolved in 10 ml of chloroform, to the solution was added 3 ml of methyl iodide at a room temperature, and the mixture was stirred for 40 minutes. Excess methyl iodide was immediately evaporated off under a reduced pressure, and resulting residue was purified on a silica gel column (silica gel 50 g, eluant: 5% methanol in chloroform), to obtain 720 mg of the title compound in a colorless amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245034
Source datasetuspto-grants-1993_09
ORD IDord-06512ce644cf455d94b7605de32b603b
Source noteuspto-grants-1993_09