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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414438Generated: November 2, 2026

Methyl iodide → N-[2-(3-amidinophenoxy)ethyl]-4-(3,4-dimethoxybenzoyl)benzamide

https://huagongshe.com/reaction/2414438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMagnesium chloride hexahydrateHCID 24644—
ReactantAmmonium AcetateHCID 517165—
ReactantN-[2-(3-cyanophenoxy)ethyl]-4-(3,4-dimethoxybenzoyl)benzamideHCID 22645151—
ReactantSodium hydrogen sulfide dihydrateHCID 86584117—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductN-[2-(3-amidinophenoxy)ethyl]-4-(3,4-dimethoxybenzoyl)benzamideHCID 9872556—

Reaction Steps

0.5 g (1.16 mmol) of N-[2-(3-cyanophenoxy)ethyl]-4-(3,4-dimethoxybenzoyl)benzamide was dissolved in 10 ml of N,N-dimethylformamide (dehydrated). 0.21 g (2.32 mmol) of sodium hydrogensulfide dihydrate and 0.24 g (1.16 mmol) of magnesium chloride hexahydrate were added to the obtained solution under cooling with ice, and they were stirred at room temperature for 2.5 hours. After the treatment with ethyl acetate as the extraction solvent in an ordinary manner, the solvent was evaporated, and the obtained crude product was dissolved in 20 ml of acetone. 0.56 ml (9.0 mmol) of methyl iodide was added to the solution, and they were refluxed for 3 hours. The solvent was evaporated, and the obtained crude product was washed with ethyl acetate. After the filtration, the obtained crystals were dissolved in 10 ml of methanol. 155 mg (2.0 mmol) of ammonium acetate was added to the obtained solution, and they were stirred for 3 hours. The solvent was evaporated, and the residue was treated in the same manner as that in step 7 in Example 51 to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812231B2
Source datasetuspto-grants-2004_11
ORD IDord-2fc9bcdb5a284233b9c94c4376d922c9
Source noteuspto-grants-2004_11