2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione

Base Information

Chemical Name:2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione
CAS No.:114060-18-3
Molecular Formula:C₂₆H₂₃N₃O₄S
Molecular Weight:473.552
Hs Code.:

Synonyms:2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione

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Chemical Property of 2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione

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Technology Process of 2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione

There total 1 articles about 2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 85-44-9
phthalic anhydride

: 114060-18-3
2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 160 °C

2: 5.4 g / H₂SO₄, HCl / 0.75 h / 0 °C

3: 35 percent / H₂SO₄ / acetic acid / 3 h / 84 °C

With hydrogenchloride; sulfuric acid; In acetic acid;
DOI:10.1021/jm00401a024

Reference yield:

: 114060-18-3
2-[4-Methoxy-2-(5-methoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-3,5-dimethyl-phenyl]-isoindole-1,3-dione

: 106747-40-4
(+)-2-[[(5-methoxy-1H-benzimidazol-2-yl)sulfinyl]methyl]-3,5-dimethyl-4-methoxybenzenamine

Guidance literature:: Multi-step reaction with 2 steps

1: 85percent m-CPBA / CH₂Cl₂ / 0.33 h / -5 °C

2: NH₂NH₂*H₂O / ethanol / 3 h / Ambient temperature

With hydrazine hydrate; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;
DOI:10.1021/jm00401a024