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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016221Generated: October 30, 2026

Methyl iodide → HCID 18406201, compound

https://huagongshe.com/reaction/1016221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Naphthalenecarboxamide, 3-hydroxy-N-[3-(4-morpholinyl)propyl]-HCID 82414—
SolventChlorobenzeneHCID 7964—
ProductHCID 18406201HCID 1840620169%

Reaction Steps

6.2 g of methyl iodide were added dropwise at 80° C. to a solution of 12.6 g of 3-hydroxynaphthalene-2-carboxylic acid (3-morpholin-4-ylpropyl)amide (RN 10155-47-2) in 60 ml of chlorobenzene. After refluxing for 4 hours, the suspension was cooled, filtered on a sinter funnel and spin-filtered. The white precipitate was washed with 20 ml of chlorobenzene and then with 20 ml of petroleum ether. The precipitate was then dried under vacuum. 12.5 g of a white solid of 4-{3-[(3-hydroxynaphthalene-2-carbonyl)amino]propyl}-4-methylmorpholin-4-ium iodide were obtained in a yield of 69%, melting at a temperature above 260° C. (Kofler) and the elemental analysis of which, calculated for C19H25N2O3.I, was:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06475247B1
Source datasetuspto-grants-2002_11
ORD IDord-9e2d3f1a839a48a0b3e3078e814db577
Source noteuspto-grants-2002_11