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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387981Generated: November 2, 2026

Methyl iodide → HCID 18472456, compound

https://huagongshe.com/reaction/1387981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 18472201HCID 18472201—
SolventDimethylformamideHCID 6228—
ProductHCID 18472456HCID 18472456—

Reaction Steps

To a solution of (E)-3-[5-(4-methylphenyl)thiophen-2-yl]-N-[4-[N-methyl-N-(tetrahydropyran-4-yl)amino-methyl]phenyl]acrylamide (100 mg) in DMF (3 ml) was added at room temperature methyl iodide (0.5 ml), and the mixture was stirred for 2 days. Under reduced pressure, the mixture was concentrated, and to the residue was added acetonitrile. The resulting crystals were collected by filtration to give yellow crystals of N,N-dimethyl-N-[4-[[(E)-3-[5-(4-methylphenyl)thiophen-2-yl]-2-propenoyl]amino]benzyl]-4-tetrahydropyranyl ammonium iodide (Compound 279) (101.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-fa9fa5099d4d4a49882bee8a9fa9acf3
Source noteuspto-grants-2001_07